Cancer Research Versailles No Abst Advances in Breast Cancer Research
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Cancer Research 67, 7534, August 1, 2007. doi: 10.1158/0008-5472.CAN-06-4275
© 2007 American Association for Cancer Research
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Newcomb, P. A.
Right arrow Articles by Potter, J. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Newcomb, P. A.
Right arrow Articles by Potter, J. D.

Epidemiology and Prevention

Estrogen Plus Progestin Use, Microsatellite Instability, and the Risk of Colorectal Cancer in Women

Polly A. Newcomb1,2,3, Yingye Zheng1, Victoria M. Chia1,2, Libby M. Morimoto1, V. Paul Doria-Rose1, Allyson Templeton1, Stephen N. Thibodeau4 and John D. Potter1,2

1 Fred Hutchinson Cancer Research Center and 2 Department of Epidemiology, University of Washington, Seattle, Washington; 3 University of Wisconsin Comprehensive Cancer Center, Madison, Wisconsin; and 4 Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, Minnesota

Requests for reprints: Polly A. Newcomb, Cancer Prevention Program, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N., P.O. Box 19024, M4-B402, Seattle, WA 98109-1024. Phone: 206-667-3476; Fax: 206-667-7850; E-mail: pnewcomb{at}fhcrc.org.


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Current users of postmenopausal hormones (PMH) have ~30% to 40% lower risk of colorectal cancer (CRC), although associations with specific types of hormones have been inconsistent. Further, it is not clear whether some tumor types have a different risk. We conducted a case-control study to examine the relationship between PMH and CRC. Cases (n = 1,004), ages 50 to 74 years, were identified from the Surveillance Epidemiology and End Results registry in Washington from 1998 to 2002; controls (n = 1,062) were randomly selected from population lists. Case tissue samples were obtained for microsatellite instability (MSI) analyses. Interviews collected risk-factor data for CRC, including detailed information on PMH. Multivariable logistic regression models estimated odds ratios (OR) and 95% confidence intervals (95% CI). Current use of any PMH was associated with a 20% reduction in CRC risk (95% CI 0.6–0.9). This reduction in risk was limited to women who had taken estrogen plus progestin (EP) preparations only (OR = 0.6, 95% CI 0.5–0.9); there was no association with estrogen-only (E alone) use (OR = 0.9, 95% CI 0.7–1.1). For women with MSI-low or MSI-stable tumors, there was a statistically significant 40% reduction in CRC risk associated with EP use (95% CI 0.4–0.9); there was no clear association with MSI-high tumors. EP use was associated with a decreased risk of CRC; however, there seemed to be no association with E alone data that are consistent with the recent Women's Health Initiative findings. Progestin may enhance the estrogenic effect of conjugated estrogen so the combination may be more biologically active in the colon than E alone. [Cancer Res 2007;67(15):7534–9]


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
Observational evidence regarding the association between exogenous hormones and colorectal cancer (CRC) in women has been remarkably consistent. In a metaanalysis, Grodstein et al. reported a statistically significant inverse relative risk of 0.66 for current users of postmenopausal hormones (PMH) compared with nonusers (1). We observed over 10 years ago that it seemed the two types of treatments [unopposed estrogen and estrogen plus progestin (EP)] yielded similar inverse effects, suggesting that estrogen was the active agent (2). A similar reduction was observed in studies of PMH and colorectal adenomas (3–8). Nonetheless, some have questioned whether PMH users simply represented a population that was healthier than women not using PMH (9, 10) and that the inverse association was, instead, due to the attributes of the users rather than the preparations themselves (9, 11). Any doubts about bias, however, were resolved by the recent results of the randomized controlled trial in the Women's Health Initiative (WHI) which found that PMH was indeed associated with a reduction in CRC risk (12). In these two studies, an important difference in effect was observed according to preparation: there was a 40% reduction in risk associated with EP use, whereas estrogen only (E alone) was not related to incidence (13). However, small numbers of CRC cases limited the interpretation.

Thus, in aggregate, epidemiologic evidence supports a protective relationship of PMH in the colorectum, yet there are many outstanding issues. Perhaps foremost is the question raised by WHI regarding the role of progestin in the colon and rectum. Further questions remain regarding specific patterns of use and subgroups, including user characteristics and tumor types, such as microsatellite unstable lesions, that may be more strongly associated with PMH use (14). We conducted a population-based case-control study to specifically evaluate the relationship between PMH type and CRC incidence.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
The study was approved by the Institutional Review Board of the Fred Hutchinson Cancer Research Center in accordance with assurances filed with and approved by the U.S. Department of Health and Human Services. Informed consent was obtained from all participants. Eligible case patients included all female residents, ages 50 to 74 years, residing in the 13 counties reporting to the Cancer Surveillance System [a population-based registry that is part of the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) program], who were newly diagnosed with invasive colorectal adenocarcinoma (International Classification of Diseases for Oncology codes C18.0, C18.2-.9, C19.9, C20.0-.9; ref. 15) between October 1998 and February 2002. Eligibility for all individuals was limited to those who were English-speaking with available telephone numbers, in which they could be contacted. On average, cases were identified within 4 months of diagnosis.

After cases were identified, physicians were contacted about their patients' eligibility for this study. If the physicians approved, the individual was approached with an introductory letter and then by a telephone call. Of the 1,414 eligible case patients identified, 141 (10%) were deceased, 66 (4%) were refused by physicians to contact, 22 (2%) could not be located, and 155 (11%) declined to participate, resulting in a final sample size of 1,030 case patients and an overall response proportion of 73%.

Community-based controls were randomly selected according to age distribution (in 5-year age intervals) of the eligible cases by using lists of licensed drivers from the Washington State Department of Licensing for individuals, ages 50 to 64 years, and rosters from the Health Care Financing Administration (now the Centers for Medicare and Medicaid) for individuals older than 64 years. Of the 1,617 potential control subjects identified, 44 (3%) were deceased, 46 (3%) could not be located, and 453 (28%) declined to participate. The final study sample included 1,074 control subjects (overall response of 66%).

We used a structured 60-min telephone interview to obtain information from all study participants on known or suspected risk factors for CRC, including use of PMH 2 years before the interview date for cases and controls. Women were asked about their use of estrogen and/or progestin, the date of use it was started, the date of use it was stopped, and total duration of use. The interview also elicited other medication use, reproductive experiences, physical activity, smoking history, selected dietary elements, height and weight, and medical history, including use of screening, family history of cancer, and demographic factors.

SEER registry reports were used to obtain information on cancer characteristics, including site, stage (local, regional, distant), and histology, along with additional demographic information. Histologic confirmation was reported for 97% of cases. For consenting cases, we collected pathology reports for a standardized review of cancer diagnoses, including site, stage, histology, grade, and distant spread.

Pathology materials. Paraffin-embedded colorectal tumors and diagnostic pathology reports were requested from a sequential sample of 757 CRC cases. Consent to acquire this material was obtained from 95% of cases, and treating institutions provided specimens for 90% of these consenting cases (n = 648). In general, sections were cut from the most representative tumor block and normal tissue block and stained with H&E. Stained sections were reviewed by site pathologist(s) and a colorectal tumor block consisting of 70% to 80% tumor cells, and a block of normal tissue were selected for further sectioning. For microsatellite instability (MSI) testing (and other future tumor DNA-based studies), ten 5-µg tumor sections were prepared. DNA was extracted from tumor and normal tissue using tissue DNA extraction kits from QIAGEN, Inc.

MSI analysis. MSI testing was completed on 590 tumors (9% had insufficient tissue for analysis) using nine markers: four mononucleotide markers (BAT25, BAT26, BAT40, and BAT34C4), four dinucleotide repeats (ACTC, D5S346, D18S55, and D10197), and one complex marker (MYCL). These markers include the five recommended markers in the panel proposed during the National Cancer Institute workshop on MSI for cancer detection (16). PCR fragments were tagged with a fluorescent dye and analyzed on an ABI3100 generic analyzer using a previously described protocol (17). For all of the cases, we corroborated the MSI results with IHC testing for hMLH1, hMSH2, and hMSH6. In a round-robin reading, this approach and interpretation has been highly reproducible.

Definitions and statistical analysis. PMH use was defined as any use for 6 months or more, and then was further divided, if possible, by type of preparation. Women were classified as E alone users if they had used estrogen exclusively for 6 months or more and had never used progestin, and as EP users if they had taken a combined preparation exclusively for 6 months or more. Women who had used both an E alone regimen and an EP regimen were included as a separate category, because the interpretation of the exposure was unclear. Current use of PMH was defined as use of hormones ~2 years before the interview date to ascertain patterns of use before diagnosis (reference date). Duration of PMH use was defined as the cumulative duration of all periods of use. Women were considered nonusers if they had never used PMH or had used PMH for <6 months. Tumors were classified as MSI-stable (MSS, 0% of loci unstable), MSI-low (>0% to <30% of loci unstable), or MSI-high (≥30% of loci unstable); unequivocal results for at least five markers were required to classify a tumor's MSI status.

Odds ratios (OR) and 95% confidence intervals (95% CI) for the association between PMH use and CRC incidence were estimated using logistic regression models, adjusting for age (in 5-year intervals), body mass index (BMI, kg/m2 in quartiles), adult onset diabetes (present, absent, or unknown), smoking status (never, former, current), regular NSAID use of 3 months or more (yes, no), colorectal screening sigmoidoscopy history within the past 10 years (yes, no, unknown), physical activity (in quartiles of hours per week), and family history of CRC (present, absent, unknown). These covariates were chosen based on a priori knowledge about risk factors for CRC. Tests of trend were conducted by including the variable in the model as an ordinal variable. To evaluate whether there were differences in the OR for E alone use versus EP use, we tested the significance of the OR for the contrast between E alone and EP using a three-level categorical covariate (never user, E alone, and EP) in the logistic model. Covariates, such as age at diagnosis, BMI, and tumor characteristics, were selected as effect modifiers because they may also influence hormone levels. Tests for interactions were assessed by a change in the log-likelihood ratio after the addition of a cross-product term between the exposure and effect modifier. Hormone use was unknown for 26 cases and 12 controls; after these exclusions, 1,004 cases and 1,062 controls remained for analysis. All statistical analyses were done using SAS v8.2 (SAS Institute, Inc.); all statistical significance tests were two-sided.


   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
The mean age was 64.2 years (range, 50–74 years) for cases and 64.5 years (range, 50–74 years) for controls. Age-adjusted selected characteristics of cases and controls are presented in Table 1 . Cases were more likely than controls to have higher BMIs (mean BMIs, 28.1 kg/m2 versus 26.7 kg/m2), adult onset diabetes, ever smoked, and to have had a family history of CRC. Among cases, MSI-high status was observed in 23.7% of tumors.


View this table:
[in this window]
[in a new window]

  		Table 1. Age-standardized characteristics (%) of women with CRC

 
For all types of PMH use, there was a statistically significant reduction in CRC risk only among current users of PMH (OR = 0.8, 95% CI 0.6–0.9), particularly among those who had used PMH for 5 years or more (Table 2 ). When stratified by type of preparation, the analysis showed no clear associations between E alone use and CRC risk regardless of recency or duration. There was even a suggestion of a slightly increased risk associated with former use of E alone (OR = 1.5, 95% CI 1.0–2.2). For women who used EP, there was no association between former use and CRC; however, current users had a 40% reduction in risk (95% CI 0.5–0.9), although this association seemed to be only present among women who used EP for 5 years or more. There was a statistically significant difference in the risk estimates for women who took E alone preparations and women who took EP (P = 0.01). When examining time since last use (Table 3 ), there were again no apparent trends between time since last E alone or EP use and CRC risk.


View this table:
[in this window]
[in a new window]

  		Table 2. Risk of CRC associated with use of PMH

 

View this table:
[in this window]
[in a new window]

  		Table 3. Association between CRC and time since last PMH use (in years), among women who used only one type of PMH

 
Associations between PMH use and CRC risk stratified by other modifiers of hormone levels are presented in Table 4 . Women, ages 70 to 74 years, had a 40% reduction in CRC risk with both E alone and EP use. For slightly younger women (60–69 years), a reduction in risk was seen with EP use but not with E alone use. For the youngest women (50–59 years), there was no reduction in risk with any type of use; indeed, there was evidence of increased risk (OR = 1.8, 95% CI 1.1–3.0) associated with use of E alone. There were no patterns in the associations between use of either type of PMH preparation and each of the following: BMI, family history, and history of distal colon screening sigmoidoscopy. Associations between CRC risk and PMH in the presence or absence of a uterus were also examined: among women with an intact uterus, there was a 30% reduction in risk in women who used EP compared with nonusers. For those without a uterus, there was no statistically significant reduction in risk (data not shown).


View this table:
[in this window]
[in a new window]

  		Table 4. Adjusted ORs of CRC and specific recent PMH use (past 10 years) according to selected characteristics

 
Associations between PMH use and CRC risk stratified by tumor characteristics are presented in Table 5 . There were no associations between MSI-high tumors and use of PMH, regardless of preparation, but for MSI-low or MSS tumors, there was a 20% (95% CI 0.6–1.0) reduction in risk associated with any PMH use and a 40% (95% CI 0.4–0.9) reduction in risk associated with EP use. These effects were, however, not statistically significantly different by MSI status (P = 0.34 for EP). Use of EP was also associated with a 40% (95% CI 0.4–1.0) reduction in tumors with a localized stage at diagnosis. For tumors diagnosed at a distant stage, any PMH use, E alone and EP, were associated with a statistically significant 40% to 50% reduction in risk. In a stratified analysis, there were no associations between E alone use and any tumor subsite. However, EP use was consistently associated with a 30% to 40% reduction in risk, regardless of tumor site.


View this table:
[in this window]
[in a new window]

  		Table 5. Adjusted ORs of specific colorectal tumor subtypes and ever use of PMH

 

   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
A differential effect of PMH was observed in this study: EP use was associated with a statistically significant inverse risk, but E alone use was not associated with CRC. Neither MSI status nor stage at diagnosis seemed to modify the associations between PMH use and CRC risk. Our confidence in these finding is enhanced by the large size of the case and control groups, the population-based nature of ascertainment, and the standardized evaluation of hormone use and other CRC risk factors. Our MSI results were further confirmed with immunohistochemistry testing, which examined expression for the most commonly known mismatch repair genes (hMLH1, hMSH2, hMSH6, hPMS2; ref. 18).

These results support previous studies of PMH and CRC by extending the sample size, preparation specific analyses, and molecular characterization of colorectal tumors. Observational evidence regarding the association between exogenous hormones and CRC in women has been remarkably consistent. Recent, pooled metaanalyses have found a consistently inverse relationship (20–40%) between PMH use and CRC risk (1, 19–21). Concerns about bias in this relationship, however, persisted until the results of the randomized controlled WHI estrogen-progestin study (12). After an average 5.2 years of follow-up, there were 45 cases of CRC in the combined EP group and 67 in the placebo arm (hazard ratio 0.63, 95% CI 0.43–0.92). In the more recently terminated E alone arm (13), the hazard ratio for CRC was 1.08; this result was based on 62 cases in the estrogen arm and there was variation by age (P = 0.048). There are important differences in the profiles of women in the two treatment arms that may have affected the results. Specifically, the E alone study enrolled slightly older women who did not have a uterus.

Evidence from WHI suggests that there may be some effect modification by age in the relationship between EP use and CRC risk; although the interaction was not statistically significant, the risk of CRC in women with ages 70 to 79 years was 0.51 compared with 0.79 in women with ages 50 to 59 years (22). We too found that the effect of EP was stronger in older women. Despite the compelling evidence from WHI, there are, nonetheless, several questions that will not be answered by that largest ever randomized controlled trial of PMH preparations. For example, because that study was stopped early, the effect of long-term use will not be known; data for whether the inverse association would be stronger among long-term users and whether it is independent of the reduction associated with recent use will not be available. It is also not known whether alternative regimens confer similar reductions in risk of CRC. To our knowledge, the only other study that has examined PMH use in relation to MSI colorectal tumors found that recent users of hormones had a reduced risk of MSI-high tumors, which we did not find in the present study; that study, however, used a different set of markers for determining MSI status (14).

The major risk factors for large bowel cancer—obesity, physical activity, and smoking—do seem to differ by sex; indeed, there is substantial evidence that these factors have a hormonal basis (23, 24). McMichael and Potter first suggested a role for estrogens and progestins in preventing colon cancer (25). Although the mechanism proposed at that time was based on changes in bile acid metabolism synthesis, the biological actions of hormones are myriad and are regulated by, among other things, their circulating concentrations, the conversion to more active or less active derivatives, and relevant receptor concentrations in the target tissue (26). In mammary tissue, provocative studies have shown that progesterone receptor-ß elicits a response to progesterone similar to that of estrogen. The biological mechanisms underlying an effect of progestins in the colon are less clear, although they may be synergistically amplifying estrogen's effects. Also, progesterone induces the isozyme of 17ß-hydroxy steroid dehydrogenase to catalyze the conversion of the less potent estrone to the more potent estradiol (27, 28). This effect has been hypothesized to explain the increased risk of breast cancer associated with EP beyond that of E alone (29). The biological mechanisms underlying an effect of progestins in the colon are less clear, although they may be synergistically amplifying estrogen's effects.

Epigenetic events not involving changes in DNA nucleotide sequences may also play a role. Estrogen and perhaps progestins may be key factors in the pathway leading to hypermethylation [CpG island methylator phenotype (CIMP); ref. 30], a central feature of CRC (31) in which many genes can be silenced. In small studies of CRC cases, an estimated 28% to 58% were CIMP+ (32–34). In vitro and animal studies have also suggested that estrogen intervention reduces DNA methylation of specific genes and restores protective methylation patterns (31).

Despite the consistency of this study with other observational and clinical trials, there are limitations that should be considered in interpreting our results. We relied, as have most observational studies, on self-reports of hormone use. We were unable to validate hormone use but other studies report good agreement of self-reported use of PMH and information in medical records (35–37). Not all eligible subjects were interviewed because of death, refusal, and other reasons; for laboratory analyses, we were not able to obtain tissue or have MSI testing completed on all individuals. We also have a higher proportion of MSI-high cases than that found in previous studies (18, 38, 39), which may indicate differences in survival by molecular subtype, an outcome that has been associated with MSI-high tumor status (40, 41).

The results of this large study support a role for exogenous hormones in the genesis of CRC in women. However, they modify the previously held belief, first postulated over 30 years ago by McMichael and Potter, that estrogen per se is the active agent in endogenous and exogenous hormone's effects (25). In future investigations the mechanisms whereby estrogens and progestins reduce risk of CRC should be explored.


   Acknowledgments
 
Grant support: National Cancer Institute, NIH grants RO1CA76366 and UO1CA74794, and cooperative agreements with members of the Colon Cancer Family Registry (C-CFR) and principal investigators.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

We thank Dr. Jeannette Bigler and Amy French for analysis of MSI; Melissa Barker and Dr. Jeremy Jass for IHC on MMR proteins; the staff of the SEER registry for assistance with data; Dr. Brenda Diergaarde for advice and consultation during the analysis; the staff of interviewers, data managers, and programmers for high-quality study data; study participants from throughout Western Washington for their generous contributions to this research; and all the C-CFR investigators for assistance with protocols and study conduct throughout this study.

The content of this manuscript does not necessarily reflect the views or policies of the National Cancer Institute or any of the collaborating institutions or investigators in the C-CFR nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. government or the C-CFR.

Received 11/20/06. Revised 3/12/07. Accepted 5/25/07.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

  1. Grodstein F, Newcomb PA, Stampfer MJ. Postmenopausal hormone therapy and the risk of colorectal cancer: a review and meta-analysis. Am J Med 1999;106:574–82.[CrossRef][Medline]
  2. Newcomb PA, Storer BE. Postmenopausal hormone use and risk of large-bowel cancer. J Natl Cancer Inst 1995;87:1067–71.[Abstract/Free Full Text]
  3. Woodson K, Lanza E, Tangrea JA, et al. Hormone replacement therapy and colorectal adenoma recurrence among women in the Polyp Prevention Trial. J Natl Cancer Inst 2001;93:1799–805.[Abstract/Free Full Text]
  4. Terry MB, Neugut AI, Bostick RM, et al. Risk factors for advanced colorectal adenomas: a pooled analysis. Cancer Epidemiol Biomarkers Prev 2002;11:622–9.[Abstract/Free Full Text]
  5. Peipins LA, Newman B, Sandler RS. Reproductive history, use of exogenous hormones, and risk of colorectal adenomas. Cancer Epidemiol Biomarkers Prev 1997;6:671–5.[Abstract/Free Full Text]
  6. Morimoto LM, Newcomb PA, Ulrich CM, et al. Risk factors for hyperplastic and adenomatous polyps: evidence for malignant potential? Cancer Epidemiol Biomarkers Prev 2002;11:1012–8.[Abstract/Free Full Text]
  7. Grodstein F, Martinez ME, Platz EA, et al. Postmenopausal hormone use and risk for colorectal cancer and adenoma. Ann Intern Med 1998;128:705–12.[Abstract/Free Full Text]
  8. Chen MJ, Longnecker MP, Morgenstern H, et al. Recent use of hormone replacement therapy and the prevalence of colorectal adenomas. Cancer Epidemiol Biomarkers Prev 1998;7:227–30.[Abstract]
  9. Matthews KA, Kuller LH, Wing RR, Meilahn EN, Plantinga P. Prior to use of estrogen replacement therapy, are users healthier than nonusers? Am J Epidemiol 1996;143:971–8.[Abstract/Free Full Text]
  10. Barrett-Connor E. Postmenopausal estrogen and prevention bias. Ann Intern Med 1991;115:455–6.[CrossRef][Medline]
  11. Sturgeon SR, Schairer C, Brinton LA, Pearson T, Hoover RN. Evidence of a healthy estrogen user survivor effect. Epidemiology 1995;6:227–31.[Medline]
  12. Rossouw JE, Anderson GL, Prentice RL, et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results From the Women's Health Initiative randomized controlled trial. JAMA 2002;288:321–33.[Abstract/Free Full Text]
  13. Anderson GL, Limacher M, Assaf AR, et al. Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: the Women's Health Initiative randomized controlled trial. JAMA 2004;291:1701–12.[Abstract/Free Full Text]
  14. Slattery ML, Potter JD, Curtin K, et al. Estrogens reduce and withdrawal of estrogens increase risk of microsatellite instability-positive colon cancer. Cancer Res 2001;61:126–30.[Abstract/Free Full Text]
  15. Percy C, Van Holten V, Muir C, editors. International Classification of Diseases for Oncology. 2nd ed. Geneva: WHO; 1990.
  16. Boland CR, Thibodeau SN, Hamilton SR, et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 1998;58:5248–57.[Abstract/Free Full Text]
  17. Lindor NM, Burgart LJ, Leontovich O, et al. Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. J Clin Oncol 2002;20:1043–8.[Abstract/Free Full Text]
  18. Grady WM. Genomic instability and colon cancer. Cancer Metastasis Rev 2004;23:11–27.[CrossRef][Medline]
  19. Nelson HD, Humphrey LL, Nygren P, Teutsch SM, Allan JD. Postmenopausal hormone replacement therapy: scientific review. JAMA 2002;288:872–81.[Abstract/Free Full Text]
  20. La Vecchia C, Gallus S, Fernandez E. Hormone replacement therapy and colorectal cancer: an update. J Br Menopause Soc 2005;11:166–72.[CrossRef][Medline]
  21. Nanda K, Bastian LA, Hasselblad V, Simel DL. Hormone replacement therapy and the risk of colorectal cancer: a meta-analysis. Obstet Gynecol 1999;93:880–8.[CrossRef][Medline]
  22. Chlebowski R, Wactawski-Wende J, Ritenbaugh C, et al. Estrogen plus progestin and colorectal cancer in postmenopausal women. N Engl J Med 2004;350:991–1004.[Abstract/Free Full Text]
  23. Tomeo CA, Colditz GA, Willet WC, et al. Harvard Report on Cancer Prevention. Volume 3: prevention of colon cancer in the United States. Cancer Causes Control 1999;10:167–80.[CrossRef][Medline]
  24. Potter JD. Colorectal cancer: molecules and populations. J Natl Cancer Inst 1999;91:916–32.[Abstract/Free Full Text]
  25. McMichael AJ, Potter JD. Reproduction, endogenous and exogenous sex hormones, and colon cancer: a review and hypothesis. J Natl Cancer Inst 1980;65:1201–7.[Medline]
  26. Foley EF, Jazaeri AA, Shupnik MA, Jazaeri O, Rice LW. Selective loss of estrogen receptor ß in malignant human colon. Cancer Res 2000;60:245–8.[Abstract/Free Full Text]
  27. Giangrande PH, Kimbrel EA, Edwards DP, McDonnell DP. The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding. Mol Cell Biol 2000;20:3102–15.[Abstract/Free Full Text]
  28. Poutanen M, Isomaa V, Peltoketo H, Vihko R. Role of 17 ß-hydroxysteroid dehydrogenase type 1 in endocrine and intracrine estradiol biosynthesis. J Steroid Biochem Mol Biol 1995;55:525–32.[CrossRef][Medline]
  29. Schairer C, Lubin J, Troisi R, et al. Menopausal estrogen and estrogen-progestin replacement therapy and breast cancer risk. JAMA 2000;283:485–91.[Abstract/Free Full Text]
  30. Baylin SB, Herman JG. DNA hypermethylation in tumorigenesis: epigenetics joins genetics. Trends Genet 2000;16:168–74.[CrossRef][Medline]
  31. Issa JP, Ottaviano YL, Celano P. Methylation of the oestrogen receptor CpG island link ageing and neoplasia in human colon. Nature Genet 1994;7:536–40.[CrossRef][Medline]
  32. Hawkins N, Norrie M, Cheong K, et al. CpG island methylation in sporadic colorectal cancers and its relationship to microsatellite instability. Gastroenterology 2002;122:1376–87.[CrossRef][Medline]
  33. Whitehall VL, Wynter CV, Walsh MD, et al. Morphological and molecular heterogeneity within nonmicrosatellite instability-high colorectal cancer. Cancer Res 2002;62:6011–4.[Abstract/Free Full Text]
  34. Toyota M, Ohe-Toyota M, Ahuja N, Issa JP. Distinct genetic profiles in colorectal tumors with or without the CpG island methylator phenotype. Proc Natl Acad Sci U S A 2000;97:710–5.[Abstract/Free Full Text]
  35. Lokkegaard EL, Johnsen SP, Heitmann BL, et al. The validity of self-reported use of hormone replacement therapy among Danish nurses. Acta Obstet Gynecol Scand 2004;83:476–81.[CrossRef][Medline]
  36. Jain MG, Rohan TE, Howe GR. Agreement of self-reported use of menopausal hormone replacement therapy with physician reports. Epidemiology 1999;10:260–3.[Medline]
  37. Goodman MT, Nomura AM, Wilkens LR, Kolonel LN. Agreement between interview information and physician records on history of menopausal estrogen use. Am J Epidemiol 1990;131:815–25.[Abstract/Free Full Text]
  38. Gryfe R, Gallinger S. Microsatellite instability, mismatch repair deficiency, and colorectal cancer. Surgery 2001;130:17–20.[CrossRef][Medline]
  39. Jacob S, Praz F. DNA mismatch repair defects: role in colorectal carcinogenesis. Biochimie 2002;84:27–47.[Medline]
  40. Popat S, Hubner R, Houlston RS. Systematic review of microsatellite instability and colorectal cancer prognosis. J Clin Oncol 2005;23:609–18.[Abstract/Free Full Text]
  41. Benatti P, Gafa R, Barana D, et al. Microsatellite instability and colorectal cancer prognosis. Clin Cancer Res 2005;11:8332–40.[Abstract/Free Full Text]



This article has been cited by other articles:


Home page
 Hum Reprod UpdateHome page
C. Bosetti, F. Bravi, E. Negri, and C. La Vecchia
Oral contraceptives and colorectal cancer risk: a systematic review and meta-analysis
Hum. Reprod. Update, May 4, 2009; (2009) dmp017v1.
[Abstract] [Full Text] [PDF]

Home page
 Cancer Epidemiol. Biomarkers Prev.Home page
R. L. Prentice, M. Pettinger, S. A.A. Beresford, J. Wactawski-Wende, F. A. Hubbell, M. L. Stefanick, and R. T. Chlebowski
Colorectal Cancer in Relation to Postmenopausal Estrogen and Estrogen Plus Progestin in the Women's Health Initiative Clinical Trial and Observational Study
Cancer Epidemiol. Biomarkers Prev., May 1, 2009; 18(5): 1531 - 1537.
[Abstract] [Full Text] [PDF]

Home page
 Cancer Res.Home page
R. Sato, T. Suzuki, Y. Katayose, K. Miura, K. Shiiba, H. Tateno, Y. Miki, J. Akahira, Y. Kamogawa, S. Nagasaki, et al.
Steroid Sulfatase and Estrogen Sulfotransferase in Colon Carcinoma: Regulators of Intratumoral Estrogen Concentrations and Potent Prognostic Factors
Cancer Res., February 1, 2009; 69(3): 914 - 922.
[Abstract] [Full Text] [PDF]

Home page
 Cancer Epidemiol. Biomarkers Prev.Home page
C. Ritenbaugh, J. L. Stanford, L. Wu, J. M. Shikany, R. E. Schoen, M. L. Stefanick, V. Taylor, C. Garland, G. Frank, D. Lane, et al.
Conjugated Equine Estrogens and Colorectal Cancer Incidence and Survival: The Women's Health Initiative Randomized Clinical Trial
Cancer Epidemiol. Biomarkers Prev., October 1, 2008; 17(10): 2609 - 2618.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Newcomb, P. A.
Right arrow Articles by Potter, J. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Newcomb, P. A.
Right arrow Articles by Potter, J. D.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online