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Breast Cancer Research


CPIC scientists studying breast cancer | Focus of our breast cancer research | Breast cancer studies | Collaborators | Products of our research

Breast cancer is the most common cancer occurring among women and the second leading cause of cancer death. Overall, breast cancer rates are very high in the Bay Area, due in some part to the lifestyle choices of our community (e.g., delayed childbearing, smaller families and greater use of hormone replacement therapyHormones (estrogen, progesterone, or both) given to women after menopause to replace the hormones no longer produced by the ovaries. Also called HRT and menopausal hormone therapy). However, our community is also very culturally diverse, so these lifestyle factors and the occurrence of breast cancer vary greatly within our community.

These circumstances compel CPIC researchers to investigate the causes, prevention, consequences, and changing patterns of breast cancer. In doing so, we focus on factors that may affect the development of breast cancer (i.e., potentially changeable as well as unchangeable aspects of lifestyle and the environment, and genetic variation) and on the experience of women after a breast cancer diagnosis (i.e., the effects of comorbiditiesComorbidity: The condition of having two or more diseases at the same time and patterns of care, and quality of life).

Our goal is to better understand the causes of this disease, its prevention and early detection, and how patients can live most successfully after a breast cancer diagnosis.

CPIC Scientists Studying Breast Cancer
The following CPIC scientists are engaged in breast cancer research (alphabetical order):

Ellen Chang, Sc.D.
Christina A. Clarke, Ph.D., M.P.H.
Sally L. Glaser, Ph.D.
Scarlett Lin Gomez, Ph.D., M.P.H.
Pamela L. Horn-Ross, Ph.D.
Esther M. John, Ph.D., M.S.P.H.
Theresa Keegan, Ph.D.
David Nelson, Ph.D.
Ingrid Oakley-Girvan, Ph.D., M.P.H.
Peggy Reynolds, Ph.D., M.P.H.
Rudy Rull, Ph.D., M.P.H.
Dee W. West, Ph.D.

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Focus of our Breast Cancer Research
CPIC scientists have been or are currently studying these breast cancer projects as well as the following aspects of breast cancer:

Incidence
Racial/ethnic differences
Birth characteristics and breast cancer in young women
Patterns and causes of geographic variation (including breast cancer in Marin County and differences between Asians in the United States and Asia)
Disease subtypes (e.g., in situIn its original place and lobular and hormone receptorA cell protein that binds a specific hormone defined tumors)
Prevalence of established risk factors
Male breast cancer

Environmental and lifestyle factors
Air quality    
Tobacco
Physical activity
Metals

Vitamin D (from diet and sunlight)

Dietary phytoestrogensAn estrogen-like substance found in some plants and plant products. Phytoestrogens may have anticancer effects (from soy, whole grains, nuts and seeds, and some fruits and vegetables)

Dietary isothiocyanates (from broccoli, cabbage, and other cruciferous vegetables)

Dietary patterns

Heterocyclic aminesAlso called HCA. A chemical that is formed when meat, poultry, or fish is cooked at high temperatures, such as frying, broiling, and barbecuing. HCA are carcinogens in cooked meat

Alcohol

Body size

Breast feeding, hormone replacement therapyHormones (estrogen, progesterone, or both) given to women after menopause to replace the hormones no longer produced by the ovaries. Also called HRT and menopausal hormone therapy, and other factors related to menstruation and reproduction

Pubertal development

Epstein-Barr virusAlso called EBV. A common virus that remains dormant in most people. It causes infectious mononucleosis and has been associated with certain cancers and other childhood infections

Immune function
Microbes and infections

Medical radiation

Migration and acculturationThe process/result of adopting the cultural traits or social patterns of another group

Occupation

Socioeconomic status and its correlates

Family history of cancer

Built environment

Genetic factors
BRCA1BRCA1 stands for breast cancer type 1. A person who inherits certain mutations in a BRCA1 gene has a higher risk of getting breast and other types of cancer, BRCA2BRCA2 stands for breast cancer type 2. A person who inherits certain mutations in a BRCA2 gene has a higher risk of getting breast and other types of cancer, ATM, CHK2
Hormone receptor genes (AR, VDR)
Immune-function genes (HLA, IL-6)
Genes determining breast density (a strong breast cancer risk factor)
Genes in the steroid hormone pathway (CYP 17, CYP 19, HSD17B1, and others)
Phase I and II genes (GST's, CYP's and others)
Alcohol metabolism genes (ADH)

Early detection
Impediments to screening
Accuracy of self-perceived risk
Risk notification among high-risk family members

Survival

Recurrence 

Clinical predictors
ComorbiditiesComorbidity: The condition of having two or more diseases at the same time (including obesity)
Racial/ethnic differences
Socioeconomic status
Male breast cancer

Treatment and cancer care issues
Quality differences in staging and adoption of new treatment regimes
Effects of age, race/ethnicity, immigration, acculturationThe process/result of adopting the cultural traits or social patterns of another group, and cultural factors
Access

Quality of life
Residual effects of treatment
Social support
Second cancers following ductal in-situ breast cancer

Studies addressing measurement issues
Dietary assessment
PhytoestrogenAn estrogen-like substance found in some plants and plant products. Phytoestrogens may have anticancer effects assessment
Validity of self-reported cancer diagnoses
Assessment of comorbidityThe condition of having two or more diseases at the same time
Race/ethnicity and birthplace classification and misclassification
Assessment of mammographic screening behavior and behavioral constructs
Socioeconomic status
High-throughput, multiplex assays for immune and infection biomarkersA biological molecule found in blood, other body fluids, or tissues that is a sign of a normal or abnormal process, or of a condition or disease
Isothiocyanate assessment

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Collaborators who Conduct Breast Cancer Research with CPIC
CPIC researchers collaborate with a variety of scientists outside of CPIC, including the following who facilitate our breast cancer research programs by providing expertise in genetic, molecular, or laboratory methods and multidisciplinary perspectives in the interpretation of results.

Collaborator Institution Expertise
Richard Ambinder, M.D., Ph.D. Johns Hopkins University VirologyThe study of viruses and viral diseases , oncologyThe study of cancer
Stephen Barnes, Ph.D. U. Alabama, Birmingham Biochemistry
Christopher Benz, M.D. U. California, San Francisco Oncology, molecular biology
Laura Esserman, M.D., M.B.A. U. California, San Francisco Oncology
Margaret Gulley, M.D. U. North Carolina Pathology
Sue Ingles, Dr.P.H. U. Southern California Genetics
Christopher Haiman, Sc.D. U. Southern California Molecular epidemiology
Alex Miron, Ph.D. Dana-Farber Cancer Institute Genetics
Hope Rugo, M.D. U. California, San Francisco Oncology
Elad Ziv, M.D. U. California, San Francisco Genetics
David Hirschberg, Ph.D. Stanford University Immunology
Allison Kurian, M.D., M.Sc. Stanford University Oncology
Julie Parsonnet, M.D. Stanford University Infectious Diseases and Epidemiology
Marcia Stefanick, Ph.D. Stanford University Cancer Prevention
Melinda Telli, M.D. Stanford University Oncology

We also collaborate with large, interdisciplinary research teams on major breast cancer projects, including the Breast Cancer Family Registry and the California Teachers Study.

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Products of our Breast Cancer Research
Our research is typically reported in the scientific literature. Since 1997, CPIC scientists have published over 60 papers reporting results of breast cancer studies in the scientific literature.

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