G. Moroni, R. Gaziano, C. Buè, M. Agostini, C. Perno, P. Sinibaldi‐Vallebona, F. Pica
{"title":"黄体酮和黑色素瘤细胞:一个悬在生与死之间的古老故事","authors":"G. Moroni, R. Gaziano, C. Buè, M. Agostini, C. Perno, P. Sinibaldi‐Vallebona, F. Pica","doi":"10.4172/2157-7536.1000158","DOIUrl":null,"url":null,"abstract":"Melanoma is a widespread cancer with poor prognosis. Female hormones are known to be capable of influencing melanoma progression but clinical data related to pregnancy, oral contraception and hormone replacement therapy are controversial. A few reports show that in vitro progesterone (PG) affects melanoma growth in nuclear progesterone receptor (nPR)-positive and nPR-negative cells, but the experimental protocols used are quite different and the results are not univocal. Further research on this topic is thus needed especially in view of the widespread use of PG in clinical practice. In this study, we used human melanoma cells (A-375), which were cultured in vitro in the presence or absence of a wide range of PG concentrations (from 0.01 to 1000 M) in single treatment. Daily cell count, cell cycle analysis and apoptosis assay were performed. Our results show that the low PG concentrations (from 0.01 to 1.0 M) promote a significant increase of melanoma cell proliferation but this growth-stimulatory effect is not observed at 10 M PG and the higher PG concentrations (i.e. 100 and 1000 M) induce a cell density reduction which is the result of both cell cycle arrest and apoptosis. These findings confirm and extend previous observations reported in the international literature. A higher caution in the clinical use of progesterone is thus mandatory, since PG concentrations capable of stimulating melanoma cell proliferation are very close to those commonly used in a wide spectrum of physio-pathological conditions.","PeriodicalId":17132,"journal":{"name":"Journal of steroids & hormonal science","volume":"51 15","pages":"1-5"},"PeriodicalIF":0.0000,"publicationDate":"2015-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"13","resultStr":"{\"title\":\"Progesterone and Melanoma Cells: An Old Story Suspended between Life and Death\",\"authors\":\"G. Moroni, R. Gaziano, C. Buè, M. Agostini, C. Perno, P. Sinibaldi‐Vallebona, F. Pica\",\"doi\":\"10.4172/2157-7536.1000158\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Melanoma is a widespread cancer with poor prognosis. Female hormones are known to be capable of influencing melanoma progression but clinical data related to pregnancy, oral contraception and hormone replacement therapy are controversial. A few reports show that in vitro progesterone (PG) affects melanoma growth in nuclear progesterone receptor (nPR)-positive and nPR-negative cells, but the experimental protocols used are quite different and the results are not univocal. Further research on this topic is thus needed especially in view of the widespread use of PG in clinical practice. In this study, we used human melanoma cells (A-375), which were cultured in vitro in the presence or absence of a wide range of PG concentrations (from 0.01 to 1000 M) in single treatment. Daily cell count, cell cycle analysis and apoptosis assay were performed. Our results show that the low PG concentrations (from 0.01 to 1.0 M) promote a significant increase of melanoma cell proliferation but this growth-stimulatory effect is not observed at 10 M PG and the higher PG concentrations (i.e. 100 and 1000 M) induce a cell density reduction which is the result of both cell cycle arrest and apoptosis. These findings confirm and extend previous observations reported in the international literature. A higher caution in the clinical use of progesterone is thus mandatory, since PG concentrations capable of stimulating melanoma cell proliferation are very close to those commonly used in a wide spectrum of physio-pathological conditions.\",\"PeriodicalId\":17132,\"journal\":{\"name\":\"Journal of steroids & hormonal science\",\"volume\":\"51 15\",\"pages\":\"1-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-08-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of steroids & hormonal science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2157-7536.1000158\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of steroids & hormonal science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2157-7536.1000158","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 13
摘要
黑色素瘤是一种广泛存在且预后不良的癌症。众所周知,女性激素能够影响黑色素瘤的进展,但与妊娠、口服避孕药和激素替代疗法相关的临床数据存在争议。一些报道表明,体外孕酮(PG)影响核孕酮受体(nPR)阳性和nPR阴性细胞的黑色素瘤生长,但使用的实验方案有很大不同,结果也不是单一的。因此,鉴于PG在临床中的广泛应用,需要对这一主题进行进一步的研究。在这项研究中,我们使用人类黑色素瘤细胞(a -375),在体外培养,在单次处理中存在或不存在广泛的PG浓度(从0.01到1000 M)。进行每日细胞计数、细胞周期分析和细胞凋亡实验。我们的研究结果表明,低浓度的PG(从0.01到1.0 M)促进了黑色素瘤细胞增殖的显著增加,但这种生长刺激作用在10 M PG时没有观察到,而较高浓度的PG(即100和1000 M)诱导细胞密度降低,这是细胞周期阻滞和凋亡的结果。这些发现证实并扩展了国际文献中报道的先前观察结果。因此,在临床使用黄体酮时必须更加谨慎,因为能够刺激黑色素瘤细胞增殖的PG浓度与广泛的生理病理条件下常用的浓度非常接近。
Progesterone and Melanoma Cells: An Old Story Suspended between Life and Death
Melanoma is a widespread cancer with poor prognosis. Female hormones are known to be capable of influencing melanoma progression but clinical data related to pregnancy, oral contraception and hormone replacement therapy are controversial. A few reports show that in vitro progesterone (PG) affects melanoma growth in nuclear progesterone receptor (nPR)-positive and nPR-negative cells, but the experimental protocols used are quite different and the results are not univocal. Further research on this topic is thus needed especially in view of the widespread use of PG in clinical practice. In this study, we used human melanoma cells (A-375), which were cultured in vitro in the presence or absence of a wide range of PG concentrations (from 0.01 to 1000 M) in single treatment. Daily cell count, cell cycle analysis and apoptosis assay were performed. Our results show that the low PG concentrations (from 0.01 to 1.0 M) promote a significant increase of melanoma cell proliferation but this growth-stimulatory effect is not observed at 10 M PG and the higher PG concentrations (i.e. 100 and 1000 M) induce a cell density reduction which is the result of both cell cycle arrest and apoptosis. These findings confirm and extend previous observations reported in the international literature. A higher caution in the clinical use of progesterone is thus mandatory, since PG concentrations capable of stimulating melanoma cell proliferation are very close to those commonly used in a wide spectrum of physio-pathological conditions.