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他莫昔芬可阻断氯离子通道。这是白内障形成的一种可能机制。

Tamoxifen blocks chloride channels. A possible mechanism for cataract formation.

作者信息

Zhang J J, Jacob T J, Valverde M A, Hardy S P, Mintenig G M, Sepúlveda F V, Gill D R, Hyde S C, Trezise A E, Higgins C F

机构信息

Department of Physiology, University of Wales, Cardiff, United Kingdom.

出版信息

J Clin Invest. 1994 Oct;94(4):1690-7. doi: 10.1172/JCI117514.

Abstract

Tamoxifen is an antiestrogen frequently used in the treatment of breast cancer and is currently being assessed as a prophylactic for those at high risk of developing tumors. We have found that tamoxifen and its derivatives are high-affinity blockers of specific chloride channels. This blockade appears to be independent of the interaction of tamoxifen with the estrogen receptor and therefore reflects an alternative cellular target. One of the clinical side effects of tamoxifen is impaired vision and cataract. Chloride channels in the lens of the eye were shown to be essential for maintaining normal lens hydration and transmittance. These channels were blocked by tamoxifen and, in organ culture, tamoxifen led to lens opacity associated with cataracts at clinically relevant concentrations. These data suggest a molecular mechanism by which tamoxifen can cause cataract formation and have implications for the clinical use of tamoxifen and related antiestrogens.

摘要

他莫昔芬是一种常用于治疗乳腺癌的抗雌激素药物,目前正在评估其作为肿瘤高危人群预防用药的效果。我们发现他莫昔芬及其衍生物是特定氯离子通道的高亲和力阻滞剂。这种阻断作用似乎独立于他莫昔芬与雌激素受体的相互作用,因此反映了另一种细胞靶点。他莫昔芬的临床副作用之一是视力受损和白内障。眼部晶状体中的氯离子通道对于维持晶状体的正常水合作用和透光率至关重要。这些通道被他莫昔芬阻断,在器官培养中,他莫昔芬在临床相关浓度下会导致与白内障相关的晶状体混浊。这些数据提示了一种他莫昔芬可导致白内障形成的分子机制,并对他莫昔芬及相关抗雌激素药物的临床应用具有启示意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8a8/295332/ace6c7e0b584/jcinvest00022-0353-a.jpg

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