Back
to BiopharmaceuticalGlossaries.com
You are here Biopharmaceutical/
Genomic
Glossary
Homepage/Search > Applications> Molecular Medicine > Cancer
diagnostics genomics prognostics & therapeutics Biopharmaceutical
Cancer diagnostics, genomics, prognostics & therapeutics glossary & taxonomy Genomic
applications Site map: Guide to terms in these
glossaries Glossaries & taxonomies Site Map Cancer has proven to be an
extraordinarily strong enemy. Biologically, the group of diseases that we
identify as cancer are distinguished by great complexity and multiple levels of
"redundancy" that enable the malignant processes to avoid attacks by
pharmaceutical agents and to re-invade the body in different ways and in
different locations. ... While progress
against cancer continues each year, the challenge remains a daunting one: to
dramatically improve our approaches to detection, diagnosis, treatment and
prevention of the second largest disease killer in the nation. caBIGTM and
Molecular Medicine, NCI, NIH http://cabig.cancer.gov/molecular/challenge.asp angiogenesis:
Cell biology
antimetabolites:
Anticancer drugs that closely resemble substances needed
by cells for normal growth. The rumor cells uses the drug instead and
"starves" for lack of proper substance. Hartford Hospital, US,
Glossary of Cancer Terms, taken from NIH Publication No.
93-2378
http://www.harthosp.org/cancer/glossary.html
apoptosis:
Cell biology artificial neural nets: Algorithms & data management
Used for classifying cancers.
autoantibodies:
A hallmark of both
autoimmunity and cancer, represent an easily accessible surrogate for measuring
adaptive immune responses to cancer. ... Serological analysis of arrays displaying the
complete human proteome (seromics)
represents a new era in cancer immunology, opening the way to defining the
repertoire of the humoral immune response to cancer. Seromic profiling of
ovarian and pancreatic cancer, Gnjatic S, et. al, Proc Natl Acad Sci U S A. 2010
Mar 16;107(11):5088-93. Epub 2010 Mar 1 http://www.ncbi.nlm.nih.gov/pubmed/20194765 biological
therapy:
A type of treatment that works with your immune system. It can help
fight cancer or help control side effects (how your body reacts to the drugs you
are taking) from other cancer treatments like chemotherapy. Biological therapy
and chemotherapy are both treatments that fight cancer. While they may seem
alike, they work in different ways. Biological therapy helps your immune system
fight cancer. Chemotherapy attacks the cancer cells directly. National
Cancer Institute, Biological Therapy http://www.cancer.gov/cancerinfo/biologicaltherapy#1
biological tumor markers:
Molecular products metabolized and secreted by neoplastic tissue and characterized biochemically in cells or body fluids. They are indicators of tumor stage and grade as well as useful for monitoring responses to treatment and predicting recurrence. Many chemical groups are represented including hormones, antigens, amino and nucleic acids, enzymes, polyamines, and specific cell membrane proteins and lipids.
MeSH, 1988 caBIG
Cancer Biomedical Informatics Grid: The National Cancer Institute is
launching a 21st century information initiative that will transform the way we
do cancer research. We are creating a network that will freely connect the
entire cancer community. In doing so, we are leveraging valuable resources and
saving precious time toward new discoveries. https://cabig.nci.nih.gov/ CGAP Cancer Genome Anatomy Project:
The goal of the NCI's Cancer Genome Anatomy Project is to determine the gene expression profiles of normal, precancer, and cancer cells, leading eventually to improved detection, diagnosis, and treatment for the patient.
CGAP, National Cancer Institute, NIH, US http://cgap.nci.nih.gov/ Cancer Biologics February 3-5, 2010
• San Francisco, CA Program
| Register | Download Brochure cancer
biomarkers: Cancer biomarkers are employed
across the entire healthcare spectrum from the cancer biological research
laboratory to patient monitoring in the clinic. Cancer biomarkers have
contributed greatly to our current understanding of the heterogeneous nature of
specific cancers and have led to improvements in treatment outcomes. Biomarker
diagnostic and drug therapy combinations are the basis of established treatment
protocols in the clinic. Insight Pharma Reports, Cancer
Biomarkers: Adoption is Driving Growth, 2008 "Cancer"
biomarkers may also be present in benign neoplastic disease, which careful
longitudinal clinical study has shown does not proceed to malignancy (13)(14). A
vitally important and humbling example is the demonstration that oncogene
markers such as c-erbB-2, p53, and cyclin D1, commonly thought to be cancer
biomarkers, are also present in patients with benign breast disease who have
been followed clinically for 15 years or longer without neoplastic progression.
... Even after more than 150 years of cell science, it must be recognized that
our conceptual framework of cancer biology remains inadequate to recognize the
ideal or optimal biomarker for most cancers. Furthermore, even if, as expected,
our perspectives will change over time, we need to understand what we are
looking for before investments in the search and evaluation for cancer
biomarkers will be effective. KP Pritzker, Cancer biomarkers: Easier said than
done, Clinical Chemistry, 48 (8): 1147- 1150 Aug. 2002 http://www.clinchem.org/cgi/content/full/48/8/1147 Cancer Biomarkers
Study Section CBSS, NIH, Center for
Scientific Review http://cms.csr.nih.gov/PeerReviewMeetings/CSRIRGDescription/ONCIRG/CBSS.htm Cancer Biomedical
Information Grid caBIG: http://cabig.nci.nih.gov/
A common, extensible informatics platform that integrates diverse data types and
supports interoperable analytic tools. This platform will allow research groups
to tap into the rich collection of emerging cancer research data while
supporting their individual investigations.
This report examines the
current status of in vivo imaging applications and in vitro cancer
diagnostic tests, as well as their future potential as important screening
tools. Cancer diagnostic technologies and assays are essential for the
detection, diagnosis, and management of cancer. For certain cancers, methods are
available for screening apparently healthy (asymptomatic) average-risk
individuals. In addition, some cancers, such as cervical and colorectal cancers,
can be detected in an even earlier, precancerous stage of development. Insight
Pharma Reports, Cancer Diagnostics: Technology and Business Trends, 2005 http://www.insightpharmareports.com/reports/2005/54_CancerDx/overview.asp cancer
fragmentomics: http://www.imss.nl/imsc17/abstracts/abstractc398.html?ID=1037 cancer genomics:
Cancer is a disease of the genome initiated by genetic mutations that alter the
functions of certain genes and their products, and advanced by accumulating
mutations that eventually transform a normal cell into a tumor cell. Using
genomics technologies such as DNA microarrays, which allow us to quantitate the
expression levels of thousands of genes simultaneously, we can comprehensively
profile gene expression patterns in human tumors and experimental models of
cancer to gain insight into the hierarchy of genes and biochemical pathways that
contribute to oncogenesis and disease progression. Cancer genomics at GIS,
Agency for Science, Technology and Research, Singapore, 2007 http://www.a-star.edu.sg/astar/biomed/action/biomed_project_details.do?id=291d284511Jv
Herceptin is an example of a drug for which specific suitable patients can now be
identified.
Oncogenomics
appears to be a synonym, but less frequently used than cancer
genomics. (Glossary
FAQ
question # 3 outlines methodology.)
Related terms: CGAP Cancer Genome Anatomy Project, familial cancer, family history, germline mutations,
oncogenomics, somatic
cells, sporadic cancer Narrower terms: cancer proteomics;
familial cancer, family
history, hereditary cancer, sporadic cancer.
Broader term: health disparities Molecular
Medicine
cancer imaging, quantitative: Molecular
Imaging
cancer immunome:
The
entire panel of expressed genes and gene products with a proven cancer
associated immunogenicity. [Ozlem Türeci, Cancer Research Institute,
Universitätskliniken des Saarlandes, Germany] http://www.cancerresearch.org/immune99/ozlem_tureci.html
Towards a Cancer Immunome Database,
Victor Jongeneel, http://www.cancerimmunity.org/v1p3/010203.htm
Broader term:
-Omes & -omics immunome; Related terms: Expression
gene & protein cancer
immunomics: The goal of our breast cancer immunomics project is to
identify new antigens that can be used for diagnostics and therapy. We
have developed a technique that allows us to efficiently identify candidate
antigens among millions of potential antigens. we are using two approaches for
this project; the first is to use blood serum from patients with breast cancer
to identify antigens that produce an immune response in patients with breast
cancer. These might be good candidates for vaccines, because the body already
creates a response, and we just have to enhance the effect. the second approach
stems from the question: Does pregnancy immunize against breast
cancer?...Finally
we have been studying immunological deficits in patients with breast cancer.
Michael Campbell, Breast Care Center, Univ. of California San Francisco http://breastcarecenter.his.ucsf.edu/newsletters/winter_2000.pdf
Broader term: -Omes & -omics
immunomics
cancer
immunotherapeutics: Cancer continues
to pose a major health burden worldwide. Prevailing therapies are extremely
limited in terms of safety, tolerability, and efficacy. Meanwhile, the morbidity
and mortality associated with cancer is fueling interest in novel therapeutic
approaches. Foremost among these are therapies that enhance the ability of the
body's own immune system to fight and destroy abnormal cancer cells. Insight
Pharma Reports Cancer
Immunotherapies and Vaccines: Pipelines Analysis and Competitive Dynamics,
2006
Recent developments
have shown successful results for an active and passive immunotherapeutic
approach to fight cancer. Modulating the immune system by either changing the
immune cells or by creating patient specific vaccines offer good opportunities
for novel pharmaceutical drug developments. Challenging areas
such as humanized monoclonal antibodies, soluble receptors, immunorepressants
and tumor treatment are seeing advances.
See also Biomarkers
cancer molecular
markers: Tissue biomarkers,
serum biomarkers, next generation sequencing as a clinical tool, microRNA
diagnostics targeting cancer, targeting cancer stem cells Cancer Profiling & Pathways
Feb
3-5 2010 San Francisco
CA Program | Register | Download Brochure
cancer resources - for
patients cancer vaccines: Cancer vaccines are intended either to treat existing
cancers (therapeutic vaccines) or to prevent the development of cancer
(prophylactic vaccines). National Cancer Institute, Treating and
Preventing Cancer with Vaccines: Introduction 2004 http://www.cancer.gov/clinicaltrials/learning/cancervaccines While
the common goal for cancer immunotherapeutics is to boost the immune system and
thereby fight cancer in various stages, what is needed most for treating cancer
successfully are more precisely-targeted therapies. The approaches vary widely
and ideally it may be reached by using the patient’s own immune system or by
inducing T-cells or “vaccines”, however, many obstacles and challenges still
need to be overcome. cellular oncogene (proto-oncogene): A
normal gene that when mutated or improperly expressed contributes to the
development of cancer. (See Oncogene.) chemoprediction:
Involves predicting the response of a specific tumor
to a range of chemotherapeutic agents. Utilizing genetic markers developed in
the collaboration should allow cancer treatments to be selected on an individual
patient basis, enabling physicians to select the most effective and least toxic
chemotherapeutic agent for each patient. Mayo Clinic and Millennium Predictive
Medicine establish strategic alliance, press release Nov, 9, 1998
Related terms: cancer genomics,
oncogenomics Biomarkers
chemotherapy: Drug
approvals and clinical trials
circulating
tumor cells: Molecular
characterization of tumour material will become increasingly important in
selecting patients for clinical trials and offering appropriate treatment for
patients in clinical practice. Recent advances in the field have indicated that
the molecular characteristics of a tumour can be determined from circulating
tumour cells and circulating tumour DNA; thus, a simple blood sample could
provide these data in a simple, convenient and efficient manner. Circulating tumour-derived predictive biomarkers
in oncology, Hodgson DR, Wellings R, Orr MC, McCormack R, Malone M, Board RE,
Cantarini MV., AstraZeneca, Drug Discov Today. 2010 Feb;15(3-4):98-101. Epub
2010 Jan 4. http://www.ncbi.nlm.nih.gov/pubmed/20045486 comparative
oncology: The study of naturally developing
cancers in animals as models for human disease. A significant and under-
utilized group of naturally occurring cancers develops in pet animals, primarily
cats and dogs. These large animal cancers share many features with human cancers
including tumor histology, genetics, response to conventional therapy and
biological behavior. Comparative Oncology Program, Center for Cancer
Research, National Cancer Institute, US http://ccr.nci.nih.gov/resources/cop/ cryochemotherapy:
By combining freezing with chemotherapy, he [Boris Rubinsky] and his colleagues
[radiologist Gary Onik and scientists from the Institut Gustave- Roussy in
Villejuif, France] hope to more precisely target malignant cells, while sparing
healthy tissue around them. Cryosurgery is performed by inserting one or more
cryoprobes, thin needles cooled with either argon gas or liquid nitrogen, into a
tumor, turning the malignant mass into an ice ball. Doctors see where they are
operating and monitor the freezing using ultrasound or magnetic resonance
imaging. Rachele Kanigel, Giving Cancer the Cold Shoulder, Forefront, College of
Engineering, Univ. of California- Berkeley http://www.coe.berkeley.edu/forefront/fall02/cancer.html Google = about 93 Sept.
23, 2004, about 390 Jan 25, 2008 diagnostics: See molecular diagnostics
dominant
(-acting) oncogene A gene that
stimulates cell proliferation and contributes to oncogenesis when present in a
single copy. See oncogene [FAO glossary]
driver mutations:
Cancer genomes carry two classes of mutations: 'driver' mutations, which are
positively selected because they are essential for tumour growth and
development, and 'passenger' mutations, which are not subject to
selection because they don't confer a growth advantage. Genomics:
Beyond the usual suspects Nature Reviews Drug
Discovery 6, 270-271
April 2007 doi:10.1038/nrd2301
endpoints, cancer
drug clinical trials: Guidance for
Industry, Clinical Trial Endpoints for the approval of cancer drugs and
biologics, Draft, FDA, 2005 http://www.fda.gov/cber/gdlns/clintrialend.pdf
epigenetics: Genetic
Manipulation & disruption extreme phenotype selection
studies:
http://www3.interscience.wiley.com/cgi-bin/abstract/98516956/ABSTRACT
familial cancer:
The expression 'familial cancer' is used
by some as a synonym of hereditary cancer, however, many (including
the authors of this program) use it simply to refer to the familial
occurrence of cancer (> 1 case in a family), not necessarily due
to an inherited cancer predisposition. Some proven hereditary disorders
include the word ‘familial’ in their name. [Familial Cancer Database On-line
Manual. R.H. Simons & G.T.N. Burger, Groningen, The Netherlands, 2000]
http://facd.uicc.org/manual.shtml
Related terms: hereditary cancer, sporadic cancer
FDA Oncology
Tools: http://www.fda.gov/cder/cancer/index.htm
fragmentome:
-Omes & -omics
galectinomics:
Knowledge about galectin expression by human tumor cells is mainly restricted to
galectins-1 and -3. This study was conducted to define the gene expression
pattern of all presently known human galectins in tumor cell lines of various
histogenetic origin. H Lahm, S Andre, A Hoeflich, JR Fischer, B Sordat, H
Kaltner, E Wolf, HJ Gabius, Comprehensive galectin fingerprinting in a panel of
61 human tumor cell lines by RT-PCR and its implications for diagnostic and
therapeutic procedures, J Cancer Res Clin Oncol. 127(6): 375- 386, 2001 http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11414198&query_hl=28 Google = about 85 Nov.
5, 2005; about 288 June 25, 2007 Gleevec:
An early example of a drug that targets a
genetic change that is characteristic of the disease being treated ... approved
for treatment of patients with chronic myeloid leukemia (CML). Gleevec inhibits
Bcr- Abl tyrosine kinase, a protein that is created by the Philadelphia
chromosome abnormality that is characteristic of CML.
Gleevec.com
http://www.gleevec.com/index.jsp
hematological cancer
pipelines: Blood cancers include
leukemia, lymphoma, and multiple myeloma. Collectively, these cancers are the
fifth most commonly occurring cancers and the second leading cause of cancer
death. The report reviews the activities of the leading companies in this arena
and provides a market assessment for all companies currently competing in or
contemplating entering the field. The major strides are being made in
small specialist companies with a broad range of compounds in Phases I– III. Insight
Pharma Reports, Hematological
Cancer Therapeutics: Pipelines and Competition, 2005 http://www.insightpharmareports.com/reports/2005/53_BloodCancer/overview.asp
Herceptin: Herceptin.com, Genentech, US http://www.herceptin.com/
A preliminary (and
promising) example of pharmacogenomics
coming into clinical use.
hereditary cancer:
The hallmark of hereditary cancer is that
the associated germ- line mutation confers a high lifetime risk of cancer
(often >50 %, but no precise risk percentage has been defined in
the literature). As a general rule, tumor development is a multi- step process
in which in addition to the germline mutation in a gene, the normal ("wild
type") copy of that gene and/ or other genes need to undergo somatic mutations
before cancer develops. [Familial Cancer Database On- line Manual. R.H.
Simons & G.T.N. Burger, Groningen, The Netherlands, 2000] http://facd.uicc.org/manual.shtml
Related
terms: familial cancer, sporadic cancer
immortalizing oncogene A gene that upon
transfection enables a primary cell to grow indefinitely in culture. [FAO
glossary]
mathematical oncology:
Clinical oncologists and
tumour biologists possess virtually no comprehensive model to serve as a
framework for understanding, organizing and applying their data... Fortunately,
there are some signs of increasing acceptance of mathematical methods in
experimental oncology. "Mathematical oncology: Cancer summed up" RA Gatenby,
PK Maini, Nature 421 (6921): 321, Jan. 23, 2003
Related term: oncologic mathematics
metagenes: Expression
gene & protein methylation:
Proteins
methylation specific PCR: Gene
amplification & PCR
methylome,
methylomics:
-Omes & omics
molecular
events: Identifying the molecular
alterations that distinguish any particular cancer cell from a normal cell will
ultimately help to define the nature and predict the pathologic behavior of that
cancer cell, as well as the responsiveness to treatment of that particular
tumor. By understanding the profile of molecular changes in any particular
cancer it will become possible to correlate the resulting phenotype of that
cancer with molecular events. Resulting knowledge will offer the potential for a
better understanding of cancer biology; the discovery of new tools and
biomarkers for detection, diagnosis, and prevention studies; and new targets for
therapeutic development. INNOVATIVE TECHNOLOGIES FOR THE MOLECULAR ANALYSIS OF
CANCER: SBIR/STTR INITIATIVE, National Cancer Institute, Release Date: May
14, 1999 http://grants.nih.gov/grants/guide/pa-files/PAR-99-101.html
molecular
imaging: Molecular imaging
molecular targets for cancer:
The Molecular Targets Development Program (MTDP) is a new organizational entity
recently launched within the Center for Cancer
Research (CCR) at NCI. ,,, The initial goal of the MTDP is to
facilitate the discovery of compounds that may serve as bioprobes for functional
genomics, proteomics and molecular target validation research, as well as leads
or candidates for drug development. Compounds of interest include not only
classical, "drug-like" organic small-molecules, but also peptides,
proteins, nucleic acids, lipids, carbohydrates and other bioactive chemical
classes. Future implementation phases of the MTDP concept may support
preclinical and clinical development of promising new molecularly targeted
investigational drugs. Molecular Targets Development Program, NCI, Center
for Cancer Research, 2003 http://home.ncifcrf.gov/mtdp/intro2.html Related terms:
molecularly targeted cancer therapies See also Drug
targets
molecular
taxonomy: There has been a lack of uniform
terminology for the precancerous and non- invasive lesions. Reasons for this
lack relate in part to changing concepts about the biology of these lesions,
subjective interpretation of criteria, heterogeneity of the neoplastic cell
population, less than optimal interobserver reproducibility, and even changes in
treatment. Very often descriptive terms applied to these lesions contain a
mixture of diagnostic and prognostic meanings. Cancer Biomarkers Research Group,
Meeting Summary Molecular Classifications for Precancerous Lesions, EDRN Working
Group, Feb. 2001, Rockville MD http://www3.cancer.gov/prevention/cbrg/molclass.html
See also
Phylogenetics molecular taxonomy
Broader term: Information
management & interpretation taxonomy
molecularly
targeted cancer therapies: Drugs that
selectively attack specific cancer-associated molecular receptors or pathways,
impeding the growth and progression of cancer.
Insight Pharma Reports, Oncogenomics, 2006 http://www.insightpharmareports.com/reports/2006/60_Oncogenomics/overview.asp
See also molecular targets for cancer neosis:
W Dr. (Raj) Rengaswami
Rajaraman, Dalhousie Univ. NuTech, Nova Universities Technology, Canada, Cancer
Biology & Therapy, Feb. 2004 http://www.landesbioscience.com/journals/cbt/abstract.php?id=663 oncogene:
A normal cellular gene which, when inappropriately
expressed or mutated, can transform eukaryotic cells into tumour cells.
[IUPAC Medicinal Chemistry]
Genes which can potentially induce neoplastic transformation. They include genes for
growth factors, growth factor receptors, protein
kinases, signal transducers, nuclear phosphoproteins, and transcription
factors. When these genes are constitutively expressed after structural and/or regulatory changes, uncontrolled cell proliferation may result. Viral oncogenes have prefix "v-" before the gene symbol; cellular oncogenes
(PROTO- ONCOGENES) have the prefix "c-" before the gene symbol.
MeSH, 1983
Narrower terms: cellular oncogenes, dominant
oncogene, immortalizing oncogene, proto-oncogene, recessive oncogene, viral
oncogenes
oncogene proteins:
Proteins coded by oncogenes.
They include proteins resulting from the fusion of an oncogene and another gene
(ONCOGENE PROTEINS, FUSION). [MeSH, 1993]
oncogenomics:
The emergence of oncogenomics promises a new era of
cancer care. Over the next decade or so, biomedical researchers hope to have
fully catalogued all genetic alterations associated with cancer, greatly
expanding the number of "druggable" anticancer molecular targets.
Oncogenomics has already seen clinical and market success with a handful of
"first-generation" oncogenomic therapeutics such as Herceptin, raising
hope and expectations that safer and more effective patient-selected targeted
therapeutics will revolutionize cancer therapy and transform cancer into a
manageable chronic disease. Insight Pharma Reports, Oncogenomics:
The future of cancer care, 2006 http://www.insightpharmareports.com/reports/2006/60_Oncogenomics/overview.asp
Insight Pharma Reports, Oncogenomics,
2006 http://www.insightpharmareports.com/reports/2006/60_Oncogenomics/overview.asp Google = about 332 July 24, 2002;
about 1,700 Sept. 8, 2003, about 7,510 Jan. 14, 2005; about 29,400 Nov 5, 2005;
about 42,100 June 25, 2007
oncologic mathematics:
HYPOTHESIS: Mathematical methods and their derivatives have practical applications to oncology. They can be used to describe fundamental aspects of tumor behavior, such as loss of genetic stability, tumor growth, immunologic identity, genesis of diversity, and methods of prognosticating cancer. DATA SOURCES:
Descriptive models and published literature in the fields of oncology and applied mathematics. DATA SYNTHESIS: Cancer does not conform to simple mathematical principles. Its irregular mode of carcinogenesis, erratic tumor growth, variable response to tumoricidal agents, and poorly understood metastatic patterns constitute highly variable clinical behavior. Defining this process requires an accurate understanding of the interactions between tumor cells and host tissues and ultimately determines prognosis. Applying
time- tested and evolving mathematical methods to oncology may provide new tools with inherent advantages for the description of tumor behavior, selection of therapeutic modes, prediction of metastatic patterns, and providing an inclusive basis for prognostication.
... CONCLUSION: Experimentally testable, oncologic mathematics may provide a framework to determine clinical outcome on a
patient- specific basis and increase the growing awareness that mathematical models help simplify seemingly complex and random tumor behavior.
"Oncologic mathematics: evolution of a new specialty" RY Chandawarkar,
DP Guyton, Archives of Surgery 137(12): 1428- 1434, Dec. 2002
Related term: mathematical oncology
oncology target discovery and
validation: Related terms: Genetic
manipulation & disruption gene silencing, knockdowns, RNAi
Oncology
Tools: http://www.fda.gov/cder/cancer/index.htm
oncolytic:
Oncolytic virotherapy is an emerging biotherapeutic platform for cancer
treatment, which is based on selective infection/killing of cancer cells by
viruses. Anticancer oncolytic activity of respiratory syncytial
virus, Echchgadda S KotaI DeLa
Cruz, A Sabbah, T Chang, R Harnack, V Mgbemena, B Chatterjee
and S Bos, Cancer Gene Therapy
(2009) 16, 923–935;
doi:10.1038/cgt.2009.34; published online 15 May 2009 oncopharmacogenomics:
Pharmacogenomics
oncoproteomics:
Proteomic
technologies are now being incorporated in oncology in the post- genomic era.
Cancer involves alterations in protein expression and provides a good model not
only for detection of biomarkers but also their use in drug discovery.
Proteomics has an impact on diagnostics as well as drug discovery. Genomics
still remains an important approach but the value of proteomics lies in the fact
that most of the diagnostics and drugs target proteins. Kewal K. Jain,
Oncoproteomics, Technology in cancer research and treatment 1(4),
Aug. 2002 http://www.tcrt.org/index.cfm?
CFID
ontologies- breast
cancer: Information management &
interpretation operomics: -Omes &
-omics
p53:
Tumor suppressor genes located on the short
arm of human chromosome 17 and coding for the phosphoprotein p53. MeSH, 1991
Broader term: tumor suppressor gene
passenger mutations:
See under driver mutations
passive
immunotherapies:
antibody products, for prevention of infection or for
treatment of many diseases, including cancer, is widespread. In addition, some
nonspecific immunomodulators on the market are used to treat certain cancers.
Insight Pharma Reports, Immunotherapies
& Vaccines for Cancer & Infectious Diseases, 2008
patient
navigation:
The Patient Navigation Research Program aims to develop
innovative patient navigation interventions to reduce or eliminate cancer health
disparities and test their efficacy and cost- effectiveness. These interventions
are designed to decrease the time between a cancer-related abnormal finding,
definitive diagnosis, and delivery of quality standard cancer care services.
Center to Reduce Cancer Health Disparities, National Cancer Institute, NIH http://crchd.cancer.gov/pnp/pnrp-index.html
Patient navigation is a
process by which an individual—a patient navigator—guides patients with a
suspicious finding (e.g, test shows they may have cancer) through and around
barriers in the complex cancer care system to help ensure timely diagnosis and
treatment.1 Barriers to quality care fall into a number of categories2:
Financial and economic, Language and
cultural, Communication, Health care system, Transportation, Bias based on
culture/race/age, Fear Pfizer Oncology, 2008 http://www.patientnavigation.com/public/PatientNavigation.aspx?LMenuId=100
pharmacomethylomics:
-Omes & - omics
predictive
oncology: Essentially promotes primary cancer
prevention by assessment of cancer susceptibility and control of genotoxic
exposures and of the basic mechanisms that may lead to the development of
neoplastic diseases. Predictive oncology incorporates also identification of
cancer prone individuals and prognostic evaluation of tumor development and
progression as well as lifestyle modification. Cancer Prediction and Prevention
Online, International Society for Preventive Oncology http://www.cancerprev.org/ISPO/About/Definition
preventive
oncology:
For secondary prevention focuses on routine clinical and
laboratory procedures for early detection and treatment of cancer, patient
management and education, management of curable lesions, education and lifestyle
modification. Involves: screening modalities and their cost effectiveness,
methodological issues of cancer detection, public awareness and professional
education, screening guidelines for cancer detection, clinical and laboratory
aspects of cancer detection, management of patients with preneoplastic
alterations, management of early curable neoplasms, novel therapeutic
approaches. Cancer Prediction and Prevention Online,
International Society for Preventive Oncology http://www.cancerprev.org/ISPO/About/Definition
proto-oncogene: See cellular oncogene
proto-oncogene proteins:
Products of
proto-oncogenes. Normally they do not have oncogenic or transforming properties,
but are involved in the regulation or differentiation of cell growth. They often
have protein kinase activity. MeSH, 1991
recessive oncogene; recessive-acting oncogene;
anti-oncogene
A single copy of this gene is
sufficient to suppress cell proliferation; the loss of both copies of the gene
contributes to cancer formation. See oncogene FAO glossary
sporadic cancer:
Cancer that occurs randomly and is not
inherited from parents. Caused by DNA changes in one cell that grows and
divides, spreading throughout the body. [DOE]
Related terms: familial cancer, family history, hereditary cancer
targeted
cancer therapies:
Targeted cancer
therapies use drugs that block the growth and spread of cancer. They interfere
with specific molecules involved in carcinogenesis (the process by which normal
cells become cancer cells) and tumor growth. Because scientists call these
molecules “molecular targets,” these therapies are sometimes called
“molecular-targeted drugs,” “molecularly targeted therapies,” or other
similar names. By focusing on molecular and cellular changes that are specific
to cancer, targeted cancer therapies may be more effective than current
treatments and less harmful to normal cells. National Cancer Institute, Targeted
Cancer Therapy Q & A, 2004 http://www.cancer.gov/cancertopics/factsheet/Therapy/targeted
Targeted
therapies: toward individualized cancer therapies, ADAPT Sept 2009 Washington DC
tumor
markers:
A substance sometimes found in an
increased amount in the blood, other body fluids, or tissues and which may mean
that a certain type of cancer is in the body. Examples of tumor markers include
CA 125 (ovarian cancer), CA 15-3 (breast cancer), CEA (ovarian, lung, breast,
pancreas, and gastrointestinal tract cancers), and PSA (prostate cancer). Also
called biomarker. [Cancer.gov dictionary]
Tumor markers
are substances, usually proteins,
that are produced by the body in response to cancer growth or by the cancer
tissue itself. Some tumor markers are specific for one type of cancer, while
others are seen in several cancer types. Many of the well-known markers are seen
in non-cancerous conditions as well as cancer. Consequently, these tumor markers
are not diagnostic for cancer. Lab Tests Online, American Association for
Clinical Chemistry in collaboration with ACLA, ASCLS, ASM, CLMA, ASH, AMP, ASCP,
NCCLS, CAP, CSLMS, CSCC, CLAS, NACB and ACB. http://www.labtestsonline.org/understanding/analytes/tumor_markers/glance.html
tumor suppressor gene:
A protective gene that normally limits
the growth of tumors. When a tumor suppressor is mutated, it may fail to
keep a cancer from growing. BRCA1 and p53 are well- known tumor suppressor
genes. [NHGRI]
Genes that inhibit expression of the tumorigenic
phenotype. They are normally involved in holding cellular growth in check. When
tumor suppressor genes are inactivated or lost, a barrier to normal
proliferation is removed and unregulated growth is possible. MeSH, 2002 Ken Kinzler and Bert Vogelstein distinguish between "gatekeeper"
tumor suppressor genes (classical) and "caretakers" (in DNA repair and
genome integrity, whose action lies outside the pathway). KW Kinzler, B.
Vogelstein "Cancer- susceptibility genes. Gatekeepers and caretakers"
Nature 386 (6627): 761, 763 Apr. 24, 1997
Narrower terms: caretaker tumor suppressor genes,
gatekeeper tumor suppressor genes, p53; Related term: Gene categories suppressor
gene
unapproved
drugs, access to: Drug approvals
Bibliography
Cancer and statistics
Stephen Jay Gould's essay "The Median isn't the Message"
is a wonderful essay on interpreting statistics and the medical literature, and
particularly useful for those of us who quickly head to a library and/ or the web with very specific and personal interest in a
medical topic. http://cancerguide.org/median_not_msg.html Robert Weinberg's Racing to the Beginning of the Road : The Search
for the Origin of Cancer 1998 is a very readable account of top
rate biomedical research, a good reminder that these "races" are marathons
and not 100 yard dashes. The title is one of my favorite metaphors for
the complexity of biology. This explanation of how nonlinear progress
from lab to clinic can be is highly recommended.
Welch, Gilbert H.
Should I Be Tested for Cancer? Univ of California Press, 2004. http://www.ucpress.edu/books/pages/10079.html
Other patient and disease related websites Genetic
& genomic testing, Patient resources
Alpha
glossary index IUPAC definitions are reprinted with the permission of
the International Union of Pure and Applied Chemistry.
Evolving Terminologies for Emerging Technologies
Comments? Questions?
Revisions? Mary Chitty mchitty@healthtech.com
Last revised August 03, 2010
<%end if%>
Related glossaries include Biomarkers
Molecular Diagnostics, Genetic & genomic testing
Molecular Medicine Pharmacogenomics
See also cancer molecular markers
Cancer
Diagnostics August
24-25, 2010 • Washington, DC Program | Register | Download Brochure

cancer proteomics:
The use of DNA microarrays to study
cancer is as established as the technology itself [5, 6]. Transcriptome
data is not only used to classify different types of cancer, but to shed light
on known and unknown cancer genes: proto- oncogenes, oncogenes, and tumor
suppressor genes. Proteome data, on the other hand, is not as pervasive,
largely due to technological limitations. However, with the steady advancements
in the tools mentioned above, “cancer proteomics” is becoming a reality.
[James Kuo "Proteomics and its applications to cancer research"
Molecular Biology & Biochemistry, Yale Univ. 2000] http://bioinfo.mbb.yale.edu/mbb452a/2000/projects/James--Kuo.html
Broader terms:
cancer immunotherapeutics 
Circulating
Tumor Cells February 23-25, 2011 • San Francisco, CA Program | Register
| Download Brochure
clinomics: Molecular
Medicine
Translational Cancer Medicine September 14-16, 2010 • Arlington,
VA Program | Register
| Download Brochure
BioMedCentral, Cancer Gateway http://www.biomedcentral.com/gateways/cancer/
caBIGTM Glossary of Terms & Definitions, Cancer Biomedical Informatics Grid,
National cancer Institute, https://cabig.nci.nih.gov/glossary
Cambridge Healthtech Associates, Cancer
Genomics: Revolutionizing Treatment and Reshaping Markets through Targeted
Therapies, 2003
Insight Pharma Reports, Cancer
Biomarkers: Adoption is Driving Growth, 2008
Insight Pharma Reports, Cancer Diagnostics: Technology and Business Trends, 2005
http://www.insightpharmareports.com/reports/2005/54_CancerDx/overview.asp
Insight Pharma Reports, Hematological
Cancer Therapeutics: Pipelines and Competition, 2005 http://www.insightpharmareports.com/reports/2005/53_BloodCancer/overview.asp
Insight Pharma Reports, Immunotherapies
& Vaccines for Cancer & Infectious Diseases, 2008
Insight Pharma Reports, Oncogenomics, 2006 http://www.insightpharmareports.com/reports/2006/60_Oncogenomics/overview.asp
IUPAC, Classification of carcinogenicity, IUPAC glossary of toxicology, 2007 http://sis.nlm.nih.gov/enviro/iupacglossary/annex3.html
NCI National Cancer Institute, Dictionary of
cancer terms, about 4,000 terms. http://www.cancer.gov/dictionary/
Updated monthly
NCI Metathesaurus Browser, National Cancer
Institute, NIH, US http://ncimeta.nci.nih.gov/MetaServlet/
Maps 3,600,000 terms from 76 sources into 1,400,000 biomedical concepts. Public
domain vocabularies from the National
Library of Medicine's UMLS
Metathesaurus, as well as a growing number of NCI-specific vocabularies
developed by the National Cancer
Institute.
NCI,
PDQ, Physicians Data Query, http://www.cancer.gov/cancer_information/pdq/
Comprehensive cancer database, Cancer information
summaries, clinical trials, links to other cancer resources
NCI Terminology
Browser, National Cancer Institute http://nciterms.nci.nih.gov/NCIBrowser/Startup.do
Can be used to view and search the NCI Thesaurus and other biomedical
vocabularies.
OncoLink, University of Pennsylvania Cancer Center
http://www.oncolink.upenn.edu/
Comprehensive information about specific types of cancer, updates on
cancer treatments and news about research advances. Updated every day,
information at various levels, from introductory to in-depth.
How
to look for other unfamiliar terms