癌症治疗的罗塞塔石碑:内源性雌激素、合成雌激素和抗雌激素抗癌能力的比较。

IF 3.1 Q2 ONCOLOGY
Zsuzsanna Suba
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引用次数: 0

摘要

这项工作提出了认识雌激素激素的主要调节能力的历史,被错误地认为是乳腺癌的促进剂超过120年。对临床、流行病学、免疫学和分子研究结果的综合分析证明,内源性雌激素是哺乳动物胚胎发育、生存和繁殖的主要调节剂,通过协调所有基因的适当表达甚至编辑。医学上使用化学修饰的合成雌激素引起毒性并发症;血栓栓塞事件和女性器官癌症风险增加,因为它们被证明是内分泌干扰物,解除了雌激素受体(er)的调节,而不是雌激素受体的激活剂。合成雌激素治疗与不同部位的癌症风险表现出模糊的相关性,这可能归因于抑制雌激素受体(er)的非配体激活以及代偿配体激活。雌激素诱发乳腺癌的原理导致了针对这种肿瘤的抗雌激素疗法的引入;雌激素受体的配体活化和芳香酶活性的抑制。最初的热情变成了失望,因为大多数乳腺癌被证明主要对抗雌激素有抗药性。此外,几乎所有早期对内分泌治疗表现出良好肿瘤反应的患者,后来都经历了导致转移性疾病和致命结局的继发性耐药。通过对抗雌激素治疗有应答和无应答肿瘤的分子事件的研究,揭示了完全抑制配体内质网的激活可以刺激肿瘤的生长,而成功的补偿性上调雌激素信号可以实现DNA的修复、肿瘤的消退和患者的生存。认识到内源性雌激素在基因表达、基因编辑和DNA修复、雌激素治疗和刺激患者ER表达中的主要作用,可能会给医疗实践带来重大转变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rosetta Stone for Cancer Cure: Comparison of the Anticancer Capacity of Endogenous Estrogens, Synthetic Estrogens and Antiestrogens.

Rosetta Stone for Cancer Cure: Comparison of the Anticancer Capacity of Endogenous Estrogens, Synthetic Estrogens and Antiestrogens.

This work presents the history of the recognition of principal regulatory capacities of estrogen hormones having been mistakenly regarded as breast cancer promoting agents for more than 120 years. Comprehensive analysis of the results of clinical, epidemiological, immunological and molecular studies justified that endogenous estrogens are the principal regulators of embryonic development, survival and reproduction via orchestrating appropriate expression and even edition of all genes in mammalians. Medical use of chemically modified synthetic estrogens caused toxic complications; thromboembolic events and increased cancer risk in female organs as they proved to be endocrine disruptors deregulating estrogen receptors (ERs) rather than their activators. Synthetic estrogen treatment exhibits ambiguous correlations with cancer risk at different sites, which may be attributed to an inhibition of the unliganded activation of estrogen receptors (ERs) coupled with compensatory liganded activation. The principle of estrogen induced breast cancer led to the introduction of antiestrogen therapies against this tumor; inhibition of the liganded activation of estrogen receptors and aromatase enzyme activity. The initial enthusiasm turned into disappointment as the majority of breast cancers proved to be primarily resistant to antiestrogens. In addition, nearly all patients showing earlier good tumor responses to endocrine therapy, later experienced secondary resistance leading to metastatic disease and fatal outcome. Studying the molecular events in tumors responsive and unresponsive to antiestrogen therapy, it was illuminated that a complete inhibition of liganded ER activation stimulates the growth of cancers, while a successful compensatory upregulation of estrogen signal may achieve DNA restoration, tumor regression and patient's survival. Recognition of the principal role of endogenous estrogens in gene expression, gene edition and DNA repair, estrogen treatment and stimulation of ER expression in patients may bring about a great turn in medical practice.

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来源期刊
Oncology Reviews
Oncology Reviews ONCOLOGY-
CiteScore
6.30
自引率
0.00%
发文量
9
审稿时长
9 weeks
期刊介绍: Oncology Reviews is a quarterly peer-reviewed, international journal that publishes authoritative state-of-the-art reviews on preclinical and clinical aspects of oncology. The journal will provide up-to-date information on the latest achievements in different fields of oncology for both practising clinicians and basic researchers. Oncology Reviews aims at being international in scope and readership, as reflected also by its Editorial Board, gathering the world leading experts in both pre-clinical research and everyday clinical practice. The journal is open for publication of supplements, monothematic issues and for publishing abstracts of scientific meetings; conditions can be obtained from the Editor-in-Chief or the publisher.
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