Evan Gibbard, Dawn R Cochrane, Ramlogan Sowamber, Jutta Huvila, Amanda S Nitschke, Kendall Greening, Christine Chow, Yimei Qin, Nissreen Mohammad, David Farnell, Wren S Lee, C Blake Gilks, Lien Hoang, Gillian E Hanley, David G Huntsman
{"title":"口服避孕药的使用与输卵管p53信号的物理大小减少有关。","authors":"Evan Gibbard, Dawn R Cochrane, Ramlogan Sowamber, Jutta Huvila, Amanda S Nitschke, Kendall Greening, Christine Chow, Yimei Qin, Nissreen Mohammad, David Farnell, Wren S Lee, C Blake Gilks, Lien Hoang, Gillian E Hanley, David G Huntsman","doi":"10.1016/j.ijgc.2025.101635","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Oral contraceptives reduce ovarian cancer risk, but the mechanism of risk reduction is not understood. We examined whether oral contraceptive pill (OCP) use influences p53 signatures, which are putative early fallopian tube precursors for high-grade serous ovarian carcinomas.</p><p><strong>Methods: </strong>For this retrospective cohort (n = 250) of subjects aged over 50 years who had fallopian tubes removed at the time of a benign gynecologic procedure, we used health records to identify 72 patients who used OCPs for at least 5 years and 178 subjects with no history of OCP use. Immunohistochemistry for p53 was performed on all fallopian tube sections, with 8 individuals removed for lack of identifiable tissue. p53 Signatures were identified and stratified based on size. Logistic regressions were run to estimate the association between OCP use and p53 lesion and lesion size.</p><p><strong>Results: </strong>There was no difference in the occurrence of p53 lesions with 20 of 70 of OCP users (28.6%) and 57 of 172 of those with no history of OCP use (33.1%). Subjects who used OCPs were more likely to have a small lesion (OR 1.98, 95% CI 1.03 to 3.83) and had decreased risk of having a medium/large lesion (OR 0.38, 95% CI 0.18 to 0.79). A total of 2 serous tubal intraepithelial lesions and 2 serous tubal intraepithelial carcinomas were identified in OCP-naive patients, whereas none were found in those with a history of OCP use.</p><p><strong>Conclusions: </strong>OCP exposure was associated with a shift toward smaller p53 lesion size but was not found to be associated with a difference in the number of p53 lesions between OCP-exposed and unexposed patients. Future research should examine whether OCP use reduces proliferation and clonal expansion of p53 signature lesions toward higher risk precursors and, eventually, cancer. There were no serous tubal intraepithelial lesions and serous tubal intraepithelial carcinomas in patients with OCP exposure.</p>","PeriodicalId":14097,"journal":{"name":"International Journal of Gynecological Cancer","volume":"35 2","pages":"101635"},"PeriodicalIF":4.7000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oral contraceptive use is associated with a reduction in the physical size of fallopian tube p53 signatures.\",\"authors\":\"Evan Gibbard, Dawn R Cochrane, Ramlogan Sowamber, Jutta Huvila, Amanda S Nitschke, Kendall Greening, Christine Chow, Yimei Qin, Nissreen Mohammad, David Farnell, Wren S Lee, C Blake Gilks, Lien Hoang, Gillian E Hanley, David G Huntsman\",\"doi\":\"10.1016/j.ijgc.2025.101635\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Oral contraceptives reduce ovarian cancer risk, but the mechanism of risk reduction is not understood. We examined whether oral contraceptive pill (OCP) use influences p53 signatures, which are putative early fallopian tube precursors for high-grade serous ovarian carcinomas.</p><p><strong>Methods: </strong>For this retrospective cohort (n = 250) of subjects aged over 50 years who had fallopian tubes removed at the time of a benign gynecologic procedure, we used health records to identify 72 patients who used OCPs for at least 5 years and 178 subjects with no history of OCP use. Immunohistochemistry for p53 was performed on all fallopian tube sections, with 8 individuals removed for lack of identifiable tissue. p53 Signatures were identified and stratified based on size. Logistic regressions were run to estimate the association between OCP use and p53 lesion and lesion size.</p><p><strong>Results: </strong>There was no difference in the occurrence of p53 lesions with 20 of 70 of OCP users (28.6%) and 57 of 172 of those with no history of OCP use (33.1%). Subjects who used OCPs were more likely to have a small lesion (OR 1.98, 95% CI 1.03 to 3.83) and had decreased risk of having a medium/large lesion (OR 0.38, 95% CI 0.18 to 0.79). A total of 2 serous tubal intraepithelial lesions and 2 serous tubal intraepithelial carcinomas were identified in OCP-naive patients, whereas none were found in those with a history of OCP use.</p><p><strong>Conclusions: </strong>OCP exposure was associated with a shift toward smaller p53 lesion size but was not found to be associated with a difference in the number of p53 lesions between OCP-exposed and unexposed patients. Future research should examine whether OCP use reduces proliferation and clonal expansion of p53 signature lesions toward higher risk precursors and, eventually, cancer. 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引用次数: 0
摘要
目的:口服避孕药降低卵巢癌风险,但降低风险的机制尚不清楚。我们研究了口服避孕药(OCP)的使用是否会影响p53信号,p53信号被认为是高级别浆液性卵巢癌的早期输卵管前体。方法:对于年龄在50岁以上且在良性妇科手术中切除输卵管的受试者(n = 250),我们使用健康记录来确定72例使用OCP至少5年的患者和178例无OCP使用史的受试者。对所有输卵管切片进行p53免疫组化,其中8例因缺乏可识别组织而切除。p53标记被识别并根据大小分层。运用Logistic回归来估计OCP使用与p53病变和病变大小之间的关系。结果:70例使用OCP者中有20例(28.6%),172例未使用OCP者中有57例(33.1%),p53病变的发生无差异。使用ocp的受试者更有可能出现小病变(OR 1.98, 95% CI 1.03至3.83),并降低发生中/大病变的风险(OR 0.38, 95% CI 0.18至0.79)。在未使用OCP的患者中共发现2例浆液管上皮内病变和2例浆液管上皮内癌,而在有OCP使用史的患者中未发现。结论:OCP暴露与p53病变变小有关,但未发现与OCP暴露与未暴露患者之间p53病变数量的差异有关。未来的研究应该检查OCP的使用是否会减少p53特征病变向高风险前体和最终癌症的增殖和克隆扩增。OCP暴露患者未见浆液管上皮内病变和浆液管上皮内癌。
Oral contraceptive use is associated with a reduction in the physical size of fallopian tube p53 signatures.
Objective: Oral contraceptives reduce ovarian cancer risk, but the mechanism of risk reduction is not understood. We examined whether oral contraceptive pill (OCP) use influences p53 signatures, which are putative early fallopian tube precursors for high-grade serous ovarian carcinomas.
Methods: For this retrospective cohort (n = 250) of subjects aged over 50 years who had fallopian tubes removed at the time of a benign gynecologic procedure, we used health records to identify 72 patients who used OCPs for at least 5 years and 178 subjects with no history of OCP use. Immunohistochemistry for p53 was performed on all fallopian tube sections, with 8 individuals removed for lack of identifiable tissue. p53 Signatures were identified and stratified based on size. Logistic regressions were run to estimate the association between OCP use and p53 lesion and lesion size.
Results: There was no difference in the occurrence of p53 lesions with 20 of 70 of OCP users (28.6%) and 57 of 172 of those with no history of OCP use (33.1%). Subjects who used OCPs were more likely to have a small lesion (OR 1.98, 95% CI 1.03 to 3.83) and had decreased risk of having a medium/large lesion (OR 0.38, 95% CI 0.18 to 0.79). A total of 2 serous tubal intraepithelial lesions and 2 serous tubal intraepithelial carcinomas were identified in OCP-naive patients, whereas none were found in those with a history of OCP use.
Conclusions: OCP exposure was associated with a shift toward smaller p53 lesion size but was not found to be associated with a difference in the number of p53 lesions between OCP-exposed and unexposed patients. Future research should examine whether OCP use reduces proliferation and clonal expansion of p53 signature lesions toward higher risk precursors and, eventually, cancer. There were no serous tubal intraepithelial lesions and serous tubal intraepithelial carcinomas in patients with OCP exposure.
期刊介绍:
The International Journal of Gynecological Cancer, the official journal of the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology, is the primary educational and informational publication for topics relevant to detection, prevention, diagnosis, and treatment of gynecologic malignancies. IJGC emphasizes a multidisciplinary approach, and includes original research, reviews, and video articles. The audience consists of gynecologists, medical oncologists, radiation oncologists, radiologists, pathologists, and research scientists with a special interest in gynecological oncology.