- Research article
- Open Access
Long-term use of calcium channel blocking drugs and breast cancer risk in a prospective cohort of US and Puerto Rican women
Breast Cancer Researchvolume 18, Article number: 61 (2016)
In a recent case–control study, long-term use of calcium channel blocking drugs was associated with a greater-than-twofold increased breast cancer risk. If prospectively collected data confirm that calcium channel blocker use increases breast cancer risk, this would have major implications for hypertension treatment. The objective of this study was to determine whether women using calcium channel blockers for 10 years or more were at increased risk of developing breast cancer compared with women not using calcium channel blockers.
The Sister Study is a prospective volunteer cohort study of women from the USA and Puerto Rico designed to evaluate environmental and genetic risk factors for breast cancer. Beginning in 2003, women between the ages of 35 and 74 were recruited. They were eligible to participate if they had a sister with breast cancer but had not been diagnosed with breast cancer themselves. In total, 50,884 women enrolled in the cohort between 2003 and 2009; 50,757 women with relevant baseline data and available follow-up data are included in this study. The exposure of interest is current use of calcium channel blocking drugs and the reported duration of use at entry into the cohort. Secondary exposures of interest were the duration and frequency of use for all other subclasses of antihypertensive drugs. Our main outcome is a self-reported diagnosis of breast cancer during the study follow-up period. With patient permission, self-reported diagnoses were confirmed using medical records.
Results showed 15,817 participants were currently using an antihypertensive drug, and 3316 women were currently using a calcium channel blocker at study baseline; 1965 women reported a breast cancer diagnosis during study follow-up. Using Cox proportional hazards modeling, we found no increased risk of breast cancer among women who had been using calcium channel blockers for 10 years or more compared with never users of calcium channel blockers (HR 0.88, 95 % CI 0.58–1.33).
We saw no evidence of increased risk of breast cancer from 10 years or more of current calcium channel blocker use. Our results do not support avoiding calcium channel blocking drugs in order to reduce breast cancer risk.
Antihypertensive drugs constitute the most commonly prescribed drug class in the USA. In 2010, Americans filled 678.2 million antihypertensive drug prescriptions [1, 2], and after starting, many individuals continue taking the drug for the rest of their lives . The association between antihypertensives and breast cancer risk has been evaluated in a limited number of studies with mixed results.
A recent case–control study of women aged 55–74 reported a twofold increased risk of breast cancer for women who were current calcium channel blocker users with at least 10 years of use . This increased risk was observed relative to women who had never used antihypertensive drugs, and relative to women using another type of antihypertensive for 10 years or more. They also reported a higher risk increase for breast cancer for women with current use of the nondihydropyridine subclass of calcium channel blockers compared with those using dihydropyridines . Several other case–control studies have also reported increased breast cancer risk in women who used calcium channel blockers [1, 3–5] or with recent use (past 2 years) of immediate-release (short-acting) calcium channel blockers  However, case–control studies are limited in their ability to establish causal risk associations; collecting exposure information after disease diagnosis may lead to recall bias. Prospective studies that assess exposure before disease diagnoses occur are effective at minimizing biases related to differential exposure recall or possible medication changes following breast cancer diagnosis and treatment. Prospective studies may also provide a more accurate picture of exposures during the at-risk period. A number of prospective cohort studies have reported no association between breast cancer and antihypertensive use in general or by drug subclass [6–13]. However, uncertainty about calcium channel blocker use and breast cancer risk remains; many of these prospective studies have been limited by small numbers of breast cancer cases, failure to examine drug subclasses, or short durations of antihypertensive use.
Contemporary prospective cohort studies with many long-term calcium channel blocker users are needed to determine whether breast cancer risk is associated with long-term use of these drugs. Although two recent cohort studies with large sample sizes did not detect increased risk of breast cancer among users of calcium channel blockers [12, 13], studies of the general population might not accurately capture elevated risks that may be amplified in women with family histories of breast cancer through interaction with other risk factors .
The Sister Study is a prospective cohort study of 50,884 women who had a sister with breast cancer and thus are at increased risk of developing breast cancer themselves. This study was designed specifically to capture possible interactions between environmental and lifestyle risk factors such as antihypertensive drug use, and the genetic risk factors underlying familial breast cancer risk. These data were collected in a time period when long-term antihypertensive use was increasingly common among women aged 50 and older, and therefore provide a unique opportunity to evaluate the effect of long-term calcium channel blocker use on breast cancer risk in a higher-risk population of women.
The Sister Study is a volunteer cohort of women recruited through media and community outreach across the USA and Puerto Rico. Women were eligible to participate if they had a sister with breast cancer and had never been diagnosed with breast cancer themselves. Between 2003 and 2009, the cohort enrolled 50,884 women and participants completed in-person physical examinations and baseline telephone interviews detailing medical, lifestyle, dietary, and reproductive history. Participants are followed for incident breast cancer diagnoses with annual health updates supplemented with detailed biennial and triennial questionnaires with follow-up response rates ≥94 % [15, 16]. The study was approved by the Institutional Review Board of the National Institute of Environmental Health Sciences, NIH and the Copernicus Group Institutional Review Board. Inclusion in this analysis is covered by the informed consent form all included cohort participants agreed to and signed.
Sister Study participants are surveyed for development of breast cancer annually, and are asked to report a new breast cancer diagnosis between follow-ups. Reported cases are confirmed with medical record retrieval. Self-reports and medical records were also used to compile and confirm information on tumor histology and hormone receptor status. At the time of analysis (Data Release 2.0), approximately 91 % of women with breast cancer consented to retrieval of their medical records. All women who reported a breast cancer diagnosis had an opportunity to disavow their report; women who disavowed their initial report of a breast cancer diagnosis (N = 3) are not included as cases in this analysis. Of the 77 % of cases (N = 1638) who had records available at the time of analysis, there was close agreement between self-report and the medical record for the diagnosis of breast cancer (99.5 %), classification of an invasive cancer (98.5 %), and ER+ status (99 %), providing a high degree of confidence in the use of self-report for those women with missing medical record data. All available breast cancer diagnoses collected during or prior to the last completed follow-up phase as of 26 April 2013 were included.
Information on use of calcium channel blocking drugs or use of other classes of antihypertensive drugs was obtained from the baseline Sister Study questionnaire. Women were asked a series of questions designed to capture information on all current and past medications for all reported medical conditions. Information on medication use collected in the survey included: the patient’s medical conditions; the name of each drug taken for the reported medical conditions; how frequently each drug was taken per week; and the first and last ages at which the drug was taken. They were also asked to report any additional medications taken that were not associated with the medical conditions they reported. To minimize reporting errors, women were asked to have their current medications on hand during the interview. They were provided booklets with the names of commonly used medications for various conditions such as hypertension prior to the interview to promote accurate reporting of current medications and medications used in the past. Each reported medication was coded by product and class using the Slone Drug Dictionary (Boston University, Boston, MA, USA). Products that contained more than one active ingredient were assigned multiple class codes.
We examined the effect of duration and class of antihypertensive drug use on breast cancer risk. We included use of antihypertensive drugs for all disease indications and reported use without a specific indication listed. Covariates were obtained from the baseline Sister Study questionnaires or measured during examiner at-home visits; these included age, race/ethnicity, underlying medical conditions and medical history, family medical history, history of benign breast conditions, smoking status, alcohol consumption habits, level of reported physical activity, body mass index (BMI) from examiner-measured height and weight, age at menarche, menopausal status, hormonal exposures including hormone replacement therapy and oral contraceptives, selected dietary factors, and history of pregnancy and breastfeeding. Baseline menopause status was determined by a women’s self-reported age at last menstrual period (LMP); a women was considered postmenopausal if 12 months or more had passed since her LMP at baseline, or if her last LMP was determined to have occurred pre baseline based on subsequent reports during study follow-up. Women with hysterectomy or uterine surgeries were considered postmenopausal when they reached the age of 56.
We characterized use of calcium channel blockers and other antihypertensive drugs in the cohort using standard contingency table methods with chi-square tests. Univariate and multivariate logistic regression analyses were used to identify potential covariates associated with different levels of current and lifetime antihypertensive use across drug subclasses. All statistical analyses were conducted using SAS 9.3 (Cary, NC, USA).
To determine the association between calcium channel blocker use and breast cancer risk, we calculated hazard ratios (HRs) for strata of lifetime use and incident breast cancer using multivariate Cox proportional hazard regression. Calcium channel blocker use was categorized into five levels: (1) never used calcium channel blocker; (2) former user of calcium channel blocker; (3) current user with less than 5 years of use; (4) current user with 5–10 years of use; and (5) current user with 10 years or more of use. The same stratifications were used for use of any type of antihypertensive drug, as well as for the following classes of antihypertensive drugs: beta-blockers, angiotensin-converting enzyme (ACE) inhibitors, diuretics, angiotensin receptor blockers, and miscellaneous drugs. Calcium channel blockers were also stratified into dihydropyridines (amlodipine, felodipine, nifedipine SR, isradipine, nifedipine, nicardipine) and nondihydropyridines (verapamil, diltiazem, verapamil SR, diltiazem XR). Women who switched from one antihypertensive drug subclass to another subclass before the baseline survey were considered former users for their previous drug subclass, current users for their current subclass, and current users of antihypertensives in general.
Attained age serves as the time scale for the Cox proportional hazards regression models. Participants enter the analysis with their age at study enrollment, and accrue person-time until they either exit at the age of breast cancer diagnosis for cases or the age at their last completed health questionnaire. Participants who failed to respond to their most recent eligible health update were censored at the earliest date among death or the midpoint of the interval between the last completed health update and the end of the window of eligibility for responding to their first missed health update. We ran crude unadjusted Cox proportional hazards regression models as well as a multivariable model with adjustment for the following variables selected as a-priori potential confounders based on existing literature: baseline-measured BMI, race/ethnicity, smoking status, parity, menopause status, age at menarche, history of breast conditions, current drinking level, hormone replacement therapy use, and statin use. We also ran models excluding women who reported prophylactic mastectomy at baseline (N = 234), or with adjustment for prophylactic tamoxifen and reloxifene use, but these factors had no material effect on our risk estimates and were excluded from the final model.
As an a-priori hypothesis, we examined risk associated with long-term use of calcium channel blocking drugs, and additionally examined use of antihypertensives in general and use of other subclasses of antihypertensive drugs. We focused on use of calcium channel blockers that lasted for 10 years or more, because this is the length of usage that has recently been associated with breast cancer risk. We also conducted analyses where long-term use was defined less strictly as 5 years or more of use to provide increased statistical power for risk detection. We examined risk associated with long-term calcium channel blocker use by breast tumor characteristics including tumor invasiveness at diagnosis and estrogen receptor status. To make our results as comparable as possible with previously conducted studies, we conducted sensitivity analyses limiting our analytical group to: women who were postmenopausal at study entry; and women who were aged 55 or older at study entry. Additionally, we conducted an active comparator sensitivity analysis in which we limited our analytical group to women who were current users of an antihypertensive drug: for at least 5 years; and for at least 10 years. This analysis allows for direct comparison of long-term calcium channel blocker users with women who were long-term users of another class of antihypertensive drug.
After excluding women missing relevant baseline or follow-up data or who were diagnosed with breast cancer before completion of enrollment activities, we had an analytical cohort of 50,757 women for this study: 17,068 women (33.6 %) reported ever taking an antihypertensive drug in their lifetime; and 15,817 (31.2 %) were currently using an antihypertensive drug, 3316 of whom were currently using a calcium channel blocker at study baseline. The majority of current antihypertensive users (90.1 %) were postmenopausal at baseline. Demographic characteristics of women who had and had not taken calcium channel blockers are presented in Table 1. On average, women who reported calcium channel blocker use were older than nonusers, with a mean age at study baseline of 60.2 years compared with a mean of 54.5 years among women who had never used calcium channel blockers (p < 0.0001). A larger proportion of calcium channel blocker users were black (21 %) compared with never users (8 %, p < 0.0001). Calcium channel blocker users had higher BMIs than nonusers (p < 0.0001) and were more likely to have used hormone replacement therapy (p < 0.0001), both of which are established risk factors for postmenopausal breast cancer. Demographics for users of all classes of antihypertensive drugs compared with nonusers were very similar to calcium channel blocker use alone (Additional file 1: Table S1).
Of the 3844 women in the cohort who reported current use of calcium channel blockers (Table 2), 820 had been using calcium channel blockers for 10 years or more. Among users of calcium channel blockers, women with longer durations of calcium channel blocker use were more likely than short-term users to be postmenopausal or to have ever used hormonal replacement therapy, both of which increase breast cancer risk (Additional file 1: Table S2).
A total of 1965 women reported a breast cancer diagnosis during study follow-up: 1372 cases of invasive breast cancer, and 558 cases that were classified as in situ, and 35 cases in which invasiveness of the tumor was unknown. The mean follow-up time for participants in the cohort was 5.3 years (SD 1.69). Of invasive cancers, 1027 were classified as invasive ductal carcinomas and 130 were invasive lobular carcinomas. Of the 558 in-situ cases, 459 were characterized as ductal carcinoma in situ (DCIS).
Calcium channel blocker use patterns and use of antihypertensive drugs in general did not differ between women who developed breast cancer during follow-up and those who remained free of breast cancer (Table 2). Of women who remained cancer free, 1.3 % had been users of calcium channel blockers for 10 years; this same percentage of women with long-term calcium channel blocker use (1.3 %) was observed among women who developed invasive breast cancer. There were no differences in the distribution of drug usage across cases and noncases for any other subclass of antihypertensive drug (Additional file 1: Table S3).
Cox proportional hazards regression showed no evidence of increased breast cancer risk with long-term calcium channel blocker use either in unadjusted models (Additional file 1: Table S4) or with adjustment for covariates (Fig. 1). Unadjusted models utilized 50,751 women with 1959 breast cancer events. Owing to missing covariate or follow-up time data, adjusted models resulted in an analytic cohort of 50,269 women, with 1933 breast cancer events. There was no increased risk of breast cancer for any duration of calcium channel blocker use when compared with women who had never used calcium channel blockers (Fig. 1). Being a current user of calcium channel blockers for 10 years or more did not increase risk of breast cancer development during follow-up compared with women who had never used calcium channel blockers (HR 0.88, 95 % CI 0.59–1.33). There was no increased risk observed when long-term use was less strictly categorized as 5 years or more of calcium channel blocker use compared with never users (HR 1.016, 95 % CI 0.78–1.32). Further stratified analysis of dihydropyridine calcium channel blockers and nondihydropyridine calcium channel blockers failed to show increased risk for either class (Additional file 1: Table S5). We also explored antihypertensive use and breast cancer risk more generally, looking at use of any antihypertensive drug (Fig. 1) and various subclasses (Additional file 1: Table S6), but found no evidence of association.
We also explored whether antihypertensive use was associated with postmenopausal breast cancers or with specific tumor subtypes. Analyses restricted to postmenopausal women (N = 38,604), women aged over 55, or stratification by ethnicity revealed no increased risk for calcium channel blocker use (Additional file 1: Figure S1). We also conducted analyses stratified by various tumor subtypes. We saw no increased risk for ER+ or ER– tumors only, nor when stratified by invasiveness status at diagnosis (Additional file 1:Supplemental Figure S1). We saw no increased risk for invasive ductal carcinoma (N = 1009 cases), for invasive lobular carcinoma (N = 130 cases), or for ductal carcinoma in situ (N = 459 cases), which were the most common types of incident breast cancers reported during follow-up (Table 3). When the analytical pool was limited to current users of antihypertensive drugs with at least 5 years of use (N = 8057) or with at least 10 years of use (N = 3879), no increased risk of breast cancer was observed with calcium channel blocker use compared with users of the other classes of antihypertensive drugs (Table 4).
Antihypertensive treatment is on the rise in the USA, with a number of different classes of therapeutic agents available. Calcium channel blockers have become an increasingly common modality of treatment over the past few decades [17, 18]. In light of the increasing prevalence of calcium channel blocker use, recent reports of its potential association with breast cancer could, if substantiated, raise serious questions on how to balance the considerable benefits of this class of agents against potential risks. While a recently conducted case–control study found an association between 10 years or more of calcium channel blocker use and invasive breast cancer , our prospective study of 50,757 women with a family history of breast cancer yielded no evidence of increased risk.
There is no strong biological rationale for increased cancer risk resulting from long-term use of calcium channel blockers. It has been hypothesized that use of calcium channel blockers may inhibit intracellular calcium channels involved in signaling and coordinating cell apoptosis . Changes in intracellular calcium concentrations are involved in response pathways to various apoptotic stimuli in many cell types, as well as in the process of DNA fragmentation during apoptosis. Interference with the apoptotic process could potentially allow tumor growth [20–22]. However, in-vivo studies and animal models have shown inconsistent relationships between calcium channel blocking drugs and apoptosis; treatment with the drugs promotes apoptosis in some cancerous and noncancerous cell types and reduces apoptosis in others [23–29]. In fact, calcium channel blocking drugs appear to have antitumorigenic properties in some situations [30–33]. This lack of convincing biological evidence is consistent with the observed lack of association between calcium channel blocker use and breast cancer risk in this study.
The study by Li et al.  was a large case–control study of women comprising 880 invasive ductal carcinoma cases, 1027 invasive lobular carcinoma cases, and 856 controls. Their exposure surveys collected detailed information on the use and duration of various classes of antihypertensive drugs. Detailed information on duration of use for subclasses of antihypertensive drugs has not been available in most contemporary studies of breast cancer, so this finding was particularly concerning. However, retrospectively collected exposure information may be subject to recall bias between women with cancer and the population-based controls. The Sister Study’s medication questionnaire method collected very similar information; however, the questionnaires in the Sister Study were administered prospectively, before any diagnosis of breast cancer occurred. Additionally, the observed risk increases in the study be Li et al. were based on a total of 70 women reporting 10 years or more of calcium channel blockers use (N = 12 controls, 27 invasive ductal carcinoma, and 31 invasive lobular carcinoma). The small number of long-term users of the calcium channel blocker subclass resulted in wide CI estimates.
Our observed lack of association between calcium channel blocker use and breast cancer risk in this Sister Study is consistent with the results of recently published analyses from the Nurse’s Health Study  and the Swedish National Board of Health and Welfare . Both of these studies used prospectively collected data from large cohorts, either from questionnaires or from Swedish Prescription Drug registries which track drug dispensations. Although the Swedish study did not have sufficient numbers of users with 10 years or more of calcium channel blocker use to evaluate risk for those women, neither study found any increased risk of breast cancer development with ever having used calcium channel blockers. We are able to extend these findings to women who are known to be at a higher risk by virtue of having an affected sister, providing additional weight to the argument that calcium channel blockers do not increase breast cancer risk.
Although a small number of women may change medications after enrollment questionnaire assessment, such changes would not be expected to bias risk estimates which are based solely on medication use up to the time of enrollment. This analysis is also limited by a relatively short mean follow-up time of 5.3 years.
While there was no association between calcium channel blocker use and development of breast cancer, we did observe that calcium channel blocker use, and use of antihypertensives in general, is associated with several breast cancer risk factors. Women who used calcium channel blockers in our study were more likely to have a history of smoking, to be overweight, to be postmenopausal, and to have used hormone replacement therapy. These associations might help to explain the inconsistencies observed in past studies of breast cancer risk and antihypertensive drug use. Incomplete adjustment for the differences in risk profiles between calcium channel blocker users and nonusers might produce associations between calcium channel blocker use and breast cancer, particularly in smaller studies.
Reports of potential excess risk due to antihypertensive drugs are likely to be of particular concern for women with increased breast cancer risk from genetic or other factors. Such concern might lead to less effective treatment for hypertension. Our findings in women with a family history of breast cancer and the findings from other recent prospective studies indicate that calcium channel blocking drugs can be used for long-term hypertension treatment without concern about increases in breast cancer risk.
ACE, angiotensin-converting enzyme; BMI, body mass index; CI, confidence interval; DCIS, ductal carcinoma in situ; ER–, estrogen receptor negative; ER+, estrogen receptor positive; HR, hazard ratio; LMP, last menstrual period; SR, sustained release; XR, extended release
Li CI, Daling JR, Tang MT, Haugen KL, Porter PL, Malone KE. Use of antihypertensive medications and breast cancer risk among women aged 55 to 74 years. JAMA Intern Med. 2013;173(17)1629–37. doi:10.1001/jamainternmed.2013.9071.
Roger VL, Go AS, Lloyd-Jones DM, Benjamin EJ, Berry JD, et al. Heart disease and stroke statistics—2012 update: a report from the American Heart Association. Circulation. 2012;125(1):e2–220. doi:10.1161/CIR.0b013e31823ac046.
Li CI, Malone KE, Weiss NS, Boudreau DM, Cushing-Haugen KL, Daling JR. Relation between use of antihypertensive medications and risk of breast carcinoma among women ages 65–79 years. Cancer. 2003;98(7):1504–13. doi:10.1002/cncr.11663.
Fitzpatrick AL, Daling JR, Furberg CD, Kronmal RA, Weissfeld JL. Use of calcium channel blockers and breast carcinoma risk in postmenopausal women. Cancer. 1997;80(8):1438–47.
Largent J, Bernstein L, Horn-Ross P, Marshall S, Neuhausen S, Reynolds P, et al. Hypertension, antihypertensive medication use, and breast cancer risk in the California Teachers Study cohort. Cancer Causes Control. 2010;21(10):1615–24. doi:10.1007/s10552-010-9590-x.
Sorensen HT, Olsen JH, Mellemkjaer L, Marie A, Steffensen FH, McLaughlin JK, et al. Cancer risk and mortality in users of calcium channel blockers. A cohort study. Cancer. 2000;89(1):165–70.
Michels KB, Rosner BA, Walker AM, Stampfer MJ, Manson JE, Colditz GA, et al. Calcium channel blockers, cancer incidence, and cancer mortality in a cohort of U.S. women: the nurses’ health study. Cancer. 1998;83(9):2003–7.
Fryzek J, Poulsen A, Lipworth L, Pedersen L, Nørgaard M, McLaughlin J, et al. A Cohort study of antihypertensive medication use and breast cancer among Danish women. Breast Cancer Res Treat. 2006;97(3):231–6. doi:10.1007/s10549-005-9091-x.
Jick H, Jick S, Derby LE, Vasilakis C, Myers MW, Meier CR. Calcium-channel blockers and risk of cancer. Lancet. 1997;349(9051):525–8. doi:10.1016/s0140-6736(97)80084-0.
Meier CR, Derby LE, Jick SS, Jick H. ANgiotensin-converting enzyme inhibitors, calcium channel blockers, and breast cancer. Arch Intern Med. 2000;160(3):349–53. doi:10.1001/archinte.160.3.349.
Olsen JH, Sorensen HT, Friis S, McLaughlin JK, Steffensen FH, Nielsen GL, et al. Cancer risk in users of calcium channel blockers. Hypertension. 1997;29(5):1091–4.
Devore EE, Kim S, Ramin CA, Wegrzyn LR, Massa J, Holmes MD, et al. Antihypertensive medication use and incident breast cancer in women. Breast Cancer Res Treat. 2015;150(1):219–29. doi:10.1007/s10549-015-3311-9.
Bergman G, Khan S, Danielsson B, Borg N. BReast cancer risk and use of calcium channel blockers using swedish population registries. JAMA Internal Med. 2014;174(10):1700–1. doi:10.1001/jamainternmed.2014.3867.
Weinberg CR, Shore DL, Umbach DM, Sandler DP. Using risk-based sampling to enrich cohorts for endpoints, genes, and exposures. Am J Epidemiol. 2007;166(4):447–55. doi:10.1093/aje/kwm097.
Xu Z, Bolick SC, Deroo LA, Weinberg CR, Sandler DP, Taylor JA. Epigenome-wide association study of breast cancer using prospectively collected Sister Study samples. J Natl Cancer Inst. 2013;105(10):694–700.
Nichols HB, Baird DD, DeRoo LA, Kissling GE, Sandler DP. Tubal ligation in relation to menopausal symptoms and breast cancer risk. Br J Cancer. 2013;109(5):1291–5. doi:10.1038/bjc.2013.433.
Gu Q, Paulose-Ram R, Dillon C, Burt V. Antihypertensive medication use among US adults with hypertension. Circulation. 2006;113(2):213–21. doi:10.1161/circulationaha.105.542290.
Gu Q, Burt VL, Dillon CF, Yoon S. Trends in antihypertensive medication use and blood pressure control among United States adults with hypertension: the National Health and Nutrition Examination Survey, 2001 to 2010. Circulation. 2012;126(17):2105–14. doi:10.1161/circulationaha.112.096156.
Daling JR. Calcium channel blockers and cancer: is an association biologically plausible? Am J Hypertens. 1996;9(7):713–4. doi:10.1016/0895-7061(96)00219-1.
Mattson MP, Chan SL. Calcium orchestrates apoptosis. Nat Cell Biol. 2003;5(12):1041–3.
Orrenius S, McConkey DJ, Bellomo G, Nicotera P. Role of Ca2+ in toxic cell killing. Trends Pharmacol Sci. 1989;10(7):281–5. doi:10.1016/0165-6147(89)90029-1.
Pinton P, Ferrari D, Rapizzi E, Virgilio FD, Pozzan T, Rizzuto R. The Ca2+ concentration of the endoplasmic reticulum is a key determinant of ceramide-induced apoptosis: significance for the molecular mechanism of Bcl-2 action. EMBO J. 2001;20(11):2690–701.
Kondo S, Yin D, Morimura T, Takeuchi J. Combination therapy with cisplatin and nifedipine inducing apoptosis in multidrug-resistant human glioblastoma cells. J Neurosurg. 1995;82(3):469–74.
Shchepotin IB, Soldatenkov V, Buras RR, Nauta RJ, Shabahang M, Evans SRT. Apoptosis of human primary and metastatic colon adenocarcinoma cell lines in vitro induced by 5-fluorouracil, verapamil, and hyperthermia. Anticancer Res. 1994;14(3 A):1027–31.
Leszczynski D, Zhao Y, Luokkamäki M, Foegh ML. Apoptosis of vascular smooth muscle cells: protein kinase C and oncoprotein Bcl-2 are involved in regulation of apoptosis in non-transformed rat vascular smooth muscle cells. Am J Pathol. 1994;145(6):1265–70.
Balakumaran A, Campbell GA, Moslen MT. Calcium channel blockers induce thymic apoptosis in vivo in rats. Toxicol Appl Pharmacol. 1996;139(1):122–7. doi:10.1006/taap.1996.0150.
Galli C, Meucci O, Scorziello A, Werge TM, Calissano P, Schettini G. Apoptosis in cerebellar granule cells is blocked by high KCl, forskolin, and IGF-1 through distinct mechanisms of action: The involvement of intracellular calcium and RNA synthesis. J Neurosci. 1995;15(2):1172–9.
Juntti-Berggren L, Larsson O, Rorsman P, Ämmälä C, Bokvist K, Wåhlander K, et al. Increased activity of L-type Ca2+ channels exposed to serum from patients with type I diabetes. Science. 1993;261(5117):86–90.
Connor J, Sawczuk IS, Benson MC, Tomashefsky P, O'Toole KM, Olsson CA, et al. Calcium channel antagonists delay regression of androgen-dependent tissues and suppress gene activity associated with cell death. Prostate. 1988;13(2):119–30.
Mason RP. Calcium channel blockers, apoptosis and cancer: is there a biologic relationship? J Am Coll Cardiol. 1999;34(7):1857–66. doi:10.1016/S0735-1097(99)00447-7.
Correale P, Tagliaferri P, Celio L, Genua G, Montagnani S, Bianco AR. Verapamil upregulates sensitivity of human colon and breast cancer cells to LAK-cytotoxicity in vitro. Eur J Cancer Clin Oncol. 1991;27(11):1393–5. doi:10.1016/0277-5379(91)90018-9.
Schüller HM, Orloff M, Reznik GK. Antiproliferative effects of the Ca2+/calmodulin antagonist B859-35 and the Ca2+-channel blocker verapamil on human lung cancer cell lines. Carcinogenesis. 1991;12(12):2301–3.
Uehara H, Nakaizumi A, Baba M, Iishi H, Tatsuta M. Inhibition by verapamil of hepatocarcinogenesis induced by N-nitrosomorpholine in Sprague-Dawley rats. Br J Cancer. 1993;68(1):37–40.
The authors wish to thank Dr Katie O’Brien and Dr Alexandra White for their critical review of this manuscript. They would also like to thank the women who volunteered to participate in the Sister Study, and all Sister Study support staff. LEW had full access to all data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
This research was supported by the Intramural Research Program of the National Institute of Environmental Health Sciences, NIH (Z01 ES044005, Z01 ES044032, and Z01 ES049033), which provided funding for design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, and approval of the manuscript.
Availability of data and materials
Because of ethical restrictions (participant confidentiality), data are available upon request. Permission to access Sister Study data may be obtained online (www.sisterstudystars.org) or by contacting the authors.
LEW conceived the study, designed and conducted statistical analyses, and wrote the manuscript. AAD contributed to the variable design, statistical analysis of the study, and the manuscript. DPS and JAT participated in the design of the study, oversaw the statistical analysis, and contributed to the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
Informed written consent was obtained from all participants prior to participation. The study was approved by the Institutional Review Boards of the National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health, and the Copernicus Group (http://www.cgirb.com/irb-services/).
Presents Supplemental Tables S1–S6 and Supplemental Figure S1. (DOCX 286 kb)