Skip to main content
Top
Published in: Breast Cancer Research 3/2002

01-06-2002 | Commentary

The contribution of inherited genotype to breast cancer

Author: Timothy R Rebbeck, PhD

Published in: Breast Cancer Research | Issue 3/2002

Login to get access

Abstract

The etiology of breast cancer is complex, and is likely to involve the actions of genes at multiple levels along the multistage carcinogenesis process. These inherited genotypes include those that affect the propensity to be exposed to breast carcinogens, and those associated with breast tumorigenesis directly. In addition, inherited genotypes may influence response to breast cancer chemoprevention and treatment. Studies relating inherited genotypes with breast cancer incidence and mortality should consider a broader spectrum of genes and their potential roles in multistage carcinogenesis than have been typically evaluated to date. Understanding the role of inherited genotype at different stages of carcinogenesis could improve our understanding of cancer biology, may identify specific exposures or events that correlate with carcinogenesis, or target relevant biochemical pathways for the development of preventive or therapeutic interventions.
Literature
1.
go back to reference Welcsh PL, King MC: BRCA1 and BRCA2 and the genetics of breast and ovarian cancer. Hum Mol Genet. 2001, 10: 705-713. 10.1093/hmg/10.7.705.CrossRefPubMed Welcsh PL, King MC: BRCA1 and BRCA2 and the genetics of breast and ovarian cancer. Hum Mol Genet. 2001, 10: 705-713. 10.1093/hmg/10.7.705.CrossRefPubMed
2.
go back to reference Lerman C, Shields PG, Audrain J, Main D, Cobb B, Boyd NR, Caporaso N: The role of the serotonin transporter gene in cigarette smoking. Cancer Epidemiol Biomarkers Prev. 1998, 7: 253-255.PubMed Lerman C, Shields PG, Audrain J, Main D, Cobb B, Boyd NR, Caporaso N: The role of the serotonin transporter gene in cigarette smoking. Cancer Epidemiol Biomarkers Prev. 1998, 7: 253-255.PubMed
3.
go back to reference Sabol SZ, Nelson ML, Fisher C, Gunzerath L, Brody CL, Hu S, Sirota LA, Marcus SE, Greenberg BD, Lucas FR, Benjamin J, Murphy DL, Hamer DH: A genetic association for cigarette smoking behavior. Health Psychol. 1999, 18: 7-13. 10.1037//0278-6133.18.1.7.CrossRefPubMed Sabol SZ, Nelson ML, Fisher C, Gunzerath L, Brody CL, Hu S, Sirota LA, Marcus SE, Greenberg BD, Lucas FR, Benjamin J, Murphy DL, Hamer DH: A genetic association for cigarette smoking behavior. Health Psychol. 1999, 18: 7-13. 10.1037//0278-6133.18.1.7.CrossRefPubMed
4.
go back to reference Lerman C, Caporaso NE, Audrain J, Main D, Bowman ED, Lockshin B, Boyd NR, Shields PG: Evidence suggesting the role of specific genetic factors in cigarette smoking. Health Psychol. 1999, 18: 14-20. 10.1037//0278-6133.18.1.14.CrossRefPubMed Lerman C, Caporaso NE, Audrain J, Main D, Bowman ED, Lockshin B, Boyd NR, Shields PG: Evidence suggesting the role of specific genetic factors in cigarette smoking. Health Psychol. 1999, 18: 14-20. 10.1037//0278-6133.18.1.14.CrossRefPubMed
5.
go back to reference Lerman C, Caporaso NE, Audrain J, Main D, Boyd NR, Shields PG: Interacting effects of the serotonin transporter gene and neuroticism in smoking practices and nicotine dependence. Mol Psychiatry. 2000, 5: 189-192. 10.1038/sj/mp/4000672.CrossRefPubMed Lerman C, Caporaso NE, Audrain J, Main D, Boyd NR, Shields PG: Interacting effects of the serotonin transporter gene and neuroticism in smoking practices and nicotine dependence. Mol Psychiatry. 2000, 5: 189-192. 10.1038/sj/mp/4000672.CrossRefPubMed
6.
go back to reference Feigelson HS, Coetzee GA, Kolonel LN, Ross RK, Henderson BE: A polymorphism in the CYP17 gene increases the risk of breast cancer. Cancer Res. 1997, 57: 1063-1065.PubMed Feigelson HS, Coetzee GA, Kolonel LN, Ross RK, Henderson BE: A polymorphism in the CYP17 gene increases the risk of breast cancer. Cancer Res. 1997, 57: 1063-1065.PubMed
7.
go back to reference Weston A, Pan CF, Bleiweiss IJ, Ksieski HB, Roy N, Maloney N, Wolff MS: CYP17 genotype and breast cancer risk. Cancer Epidemiol Biomarkers Prev. 1998, 7: 941-944.PubMed Weston A, Pan CF, Bleiweiss IJ, Ksieski HB, Roy N, Maloney N, Wolff MS: CYP17 genotype and breast cancer risk. Cancer Epidemiol Biomarkers Prev. 1998, 7: 941-944.PubMed
8.
go back to reference Helzlsouer KJ, Huang HY, Strickland PT, Hoffman S, Alberg AJ, Comstock GW, Bell DA: Association between CYP17 polymorphisms and the development of breast cancer. Cancer Epidemiol Biomarkers Prev. 1998, 7: 945-949.PubMed Helzlsouer KJ, Huang HY, Strickland PT, Hoffman S, Alberg AJ, Comstock GW, Bell DA: Association between CYP17 polymorphisms and the development of breast cancer. Cancer Epidemiol Biomarkers Prev. 1998, 7: 945-949.PubMed
9.
go back to reference Haiman CA, Hankinson SE, Spiegelman D, Colditz GA, Willett WC, Speizer FE, Kelsey KT, Hunter DJ: The relationship between a polymorphism in CYP17 with plasma hormone levels and breast cancer. Cancer Res. 1999, 59: 1015-1020.PubMed Haiman CA, Hankinson SE, Spiegelman D, Colditz GA, Willett WC, Speizer FE, Kelsey KT, Hunter DJ: The relationship between a polymorphism in CYP17 with plasma hormone levels and breast cancer. Cancer Res. 1999, 59: 1015-1020.PubMed
10.
go back to reference Dehal SS, Kupfer D: CYP2D6 catalyzes tamoxifen 4-hydroxylation in human liver. Cancer Res. 1997, 57: 3402-3406.PubMed Dehal SS, Kupfer D: CYP2D6 catalyzes tamoxifen 4-hydroxylation in human liver. Cancer Res. 1997, 57: 3402-3406.PubMed
11.
go back to reference Jacolot F, Simon I, Dreano Y, Beaune P, Riche C, Berthou F: Identification of the cytochrome P450 IIIA family as the enzymes involved in the N-demethylation of tamoxifen in human liver microsomes. Biochem Pharmacol. 1991, 41: 1911-1919. 10.1016/0006-2952(91)90131-N.CrossRefPubMed Jacolot F, Simon I, Dreano Y, Beaune P, Riche C, Berthou F: Identification of the cytochrome P450 IIIA family as the enzymes involved in the N-demethylation of tamoxifen in human liver microsomes. Biochem Pharmacol. 1991, 41: 1911-1919. 10.1016/0006-2952(91)90131-N.CrossRefPubMed
12.
go back to reference Schulte PA, Perera FP, Ed: Molecular Epidemiology: Principles and Practices. San Diego: Academic Press;. 1993 Schulte PA, Perera FP, Ed: Molecular Epidemiology: Principles and Practices. San Diego: Academic Press;. 1993
13.
go back to reference Sing CF, Boerwinkle E, Turner ST: Genetics of primary hypertension. Clin Exp Hypertens A. 1986, 8: 623-651.PubMed Sing CF, Boerwinkle E, Turner ST: Genetics of primary hypertension. Clin Exp Hypertens A. 1986, 8: 623-651.PubMed
14.
go back to reference Rebbeck TR, Kantoff PA, Krithivas K, Godwin AK, Daly MB, Narod SA, Garber JE, Weber BL, Brown M: Modification of BRCA1-associated breast cancer penetrance by androgen receptor CAG repeat length variants. Am J Human Genet. 1999, 64: 1371-1377. 10.1086/302366.CrossRef Rebbeck TR, Kantoff PA, Krithivas K, Godwin AK, Daly MB, Narod SA, Garber JE, Weber BL, Brown M: Modification of BRCA1-associated breast cancer penetrance by androgen receptor CAG repeat length variants. Am J Human Genet. 1999, 64: 1371-1377. 10.1086/302366.CrossRef
15.
go back to reference Rebbeck TR, Wang Y, Kantoff PW, Krithivas K, Neuhausen S, Godwin AK, Daly MB, Narod SA, Brunet J-S, Vesprini D, Garber JE, Lynch HT, Weber BL, Brown M: Modification of BRCA1- and BRCA2-associated breast cancer risk by AIB1 genotype and reproductive history. Cancer Research. 2001, 61: 5420-5424.PubMed Rebbeck TR, Wang Y, Kantoff PW, Krithivas K, Neuhausen S, Godwin AK, Daly MB, Narod SA, Brunet J-S, Vesprini D, Garber JE, Lynch HT, Weber BL, Brown M: Modification of BRCA1- and BRCA2-associated breast cancer risk by AIB1 genotype and reproductive history. Cancer Research. 2001, 61: 5420-5424.PubMed
16.
go back to reference Thomas DC: Design of gene characterization studies: an overview. J Natl Cancer Inst Monogr. 1999, 26: 17-23.CrossRef Thomas DC: Design of gene characterization studies: an overview. J Natl Cancer Inst Monogr. 1999, 26: 17-23.CrossRef
17.
go back to reference Caporaso N, Rothman N, Wacholder S: Case-control studies of common alleles and environmental factors. J Natl Cancer Inst Mongr. 1999, 26: 25-30.CrossRef Caporaso N, Rothman N, Wacholder S: Case-control studies of common alleles and environmental factors. J Natl Cancer Inst Mongr. 1999, 26: 25-30.CrossRef
18.
go back to reference Langholz B, Rothman N, Wacholder S, Thomas DC: Cohort studies for characterizing measured genes. J Natl Cancer Inst Monogr. 1999, 26: 39-42.CrossRef Langholz B, Rothman N, Wacholder S, Thomas DC: Cohort studies for characterizing measured genes. J Natl Cancer Inst Monogr. 1999, 26: 39-42.CrossRef
19.
go back to reference Gauderman WJ, Witte JS, Thomas DC: Family-based association studies. J Natl Cancer Inst Monogr. 1999, 26: 31-37.CrossRef Gauderman WJ, Witte JS, Thomas DC: Family-based association studies. J Natl Cancer Inst Monogr. 1999, 26: 31-37.CrossRef
20.
go back to reference Goldstein AM, Andrieu N: Detection of interaction involving identified genes: available study designs. J Natl Cancer Inst Monogr. 1999, 26: 49-54.CrossRef Goldstein AM, Andrieu N: Detection of interaction involving identified genes: available study designs. J Natl Cancer Inst Monogr. 1999, 26: 49-54.CrossRef
21.
go back to reference Krynetski EV, Evans WE: Genetic polymorphism of thiopurine S-methyltransferase: molecular mechanisms and clinical importance. Pharmacology. 2000, 61: 136-146. 10.1159/000028394.CrossRefPubMed Krynetski EV, Evans WE: Genetic polymorphism of thiopurine S-methyltransferase: molecular mechanisms and clinical importance. Pharmacology. 2000, 61: 136-146. 10.1159/000028394.CrossRefPubMed
22.
go back to reference Krynetski EY, Tai HL, Yates CR, Fessing MY, Loennechen T, Schuetz JD, Relling MV, Evans WE: Genetic polymorphism of thiopurine S-methyltransferase: clinical importance and molecular mechanisms. Pharmacogenetics. 1996, 6: 279-290.CrossRefPubMed Krynetski EY, Tai HL, Yates CR, Fessing MY, Loennechen T, Schuetz JD, Relling MV, Evans WE: Genetic polymorphism of thiopurine S-methyltransferase: clinical importance and molecular mechanisms. Pharmacogenetics. 1996, 6: 279-290.CrossRefPubMed
23.
go back to reference Otterness D, Szumlanski C, Lennard L, Klemetsdal B, Aarbakke J, Park-Hah JO, Iven H, Schmiegelow K, Branum E, O'Brien J, Wein-shilboum R: Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms. Clin Pharmacol Ther. 1997, 62: 60-73.CrossRefPubMed Otterness D, Szumlanski C, Lennard L, Klemetsdal B, Aarbakke J, Park-Hah JO, Iven H, Schmiegelow K, Branum E, O'Brien J, Wein-shilboum R: Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms. Clin Pharmacol Ther. 1997, 62: 60-73.CrossRefPubMed
24.
go back to reference Iyer L, Ratain MJ: Pharmacogenetics and cancer chemotherapy. Eur J Cancer. 1998, 34: 1493-1499. 10.1016/S0959-8049(98)00230-5.CrossRefPubMed Iyer L, Ratain MJ: Pharmacogenetics and cancer chemotherapy. Eur J Cancer. 1998, 34: 1493-1499. 10.1016/S0959-8049(98)00230-5.CrossRefPubMed
25.
go back to reference Menard S, Fortis S, Castiglioni F, Agresti R, Balsari A: HER2 as a prognostic factor in breast cancer. Oncology. 2001, 61 (suppl 2): 67-72.CrossRefPubMed Menard S, Fortis S, Castiglioni F, Agresti R, Balsari A: HER2 as a prognostic factor in breast cancer. Oncology. 2001, 61 (suppl 2): 67-72.CrossRefPubMed
Metadata
Title
The contribution of inherited genotype to breast cancer
Author
Timothy R Rebbeck, PhD
Publication date
01-06-2002
Publisher
BioMed Central
Published in
Breast Cancer Research / Issue 3/2002
Electronic ISSN: 1465-542X
DOI
https://doi.org/10.1186/bcr430

Other articles of this Issue 3/2002

Breast Cancer Research 3/2002 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine