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Diverse pathomechanisms leading to the breakdown of cellular estrogen surveillance and breast cancer development: new therapeutic strategies

机译:导致细胞雌激素监测和乳腺癌发展崩溃的多种病理机制:新的治疗策略

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Abstract: Recognition of the two main pathologic mechanisms equally leading to breast cancer development may provide explanations for the apparently controversial results obtained by sexual hormone measurements in breast cancer cases. Either insulin resistance or estrogen receptor (ER) defect is the initiator of pathologic processes and both of them may lead to breast cancer development. Primary insulin resistance induces hyperandrogenism and estrogen deficiency, but during these ongoing pathologic processes, ER defect also develops. Conversely, when estrogen resistance is the onset of hormonal and metabolic disturbances, initial counteraction is hyperestrogenism. Compensatory mechanisms improve the damaged reactivity of ERs; however, their failure leads to secondary insulin resistance. The final stage of both pathologic pathways is the breakdown of estrogen surveillance, leading to breast cancer development. Among premenopausal breast cancer cases, insulin resistance is the preponderant initiator of alterations with hyperandrogenism, which is reflected by the majority of studies suggesting a causal role of hyperandrogenism in breast cancer development. In the majority of postmenopausal cases, tumor development may also be initiated by insulin resistance, while hyperandrogenism is typically coupled with elevated estrogen levels within the low postmenopausal hormone range. This mild hyperestrogenism is the remnant of reactive estrogen synthesis against refractory ERs that were successfully counteracted at a younger age. When refractoriness of ERs is the initiator of pathologic processes, reactively increased estrogen levels may be found in both young and older breast cancer cases, while they may exhibit clinical symptoms of estrogen deficiency. Studies justifying a causal correlation between hyperestrogenism and tumor development compile such breast cancer cases. In conclusion, the quantitative evaluation of ER refractoriness in breast cancer cases has great importance, since the stronger the estrogen resistance, the higher the promising dose of estrogen therapy.
机译:摘要:对导致乳腺癌发展的两种主要病理机制的认识可能为乳腺癌病例中性激素测量获得的明显争议性结果提供了解释。胰岛素抵抗或雌激素受体(ER)缺陷都是病理过程的发起者,两者都可能导致乳腺癌的发展。原发性胰岛素抵抗会引起雄激素过多和雌激素缺乏,但是在这些正在进行的病理过程中,ER缺陷也会发展。相反,当雌激素抵抗是激素和代谢紊乱的发作时,最初的对抗作用就是雌激素过多症。补偿机制改善了ER的受损反应性;然而,它们的失败导致继发胰岛素抵抗。两种病理途径的最后阶段都是雌激素监测的崩溃,导致乳腺癌的发展。在绝经前的乳腺癌病例中,胰岛素抵抗是高雄激素血症发生改变的主要诱因,这表明大多数研究表明高雄激素血症在乳腺癌发展中具有因果作用。在绝经后的大多数病例中,肿瘤的发展也可能由胰岛素抵抗引起,而雄激素过多通常与绝经后激素水平低下的雌激素水平升高有关。这种轻微的雌激素过多是抵抗难治性ER的反应性雌激素合成的残留物,这些抗性ER在年轻时已被成功抵消。当ERs的难治性是病理过程的发起者时,在年轻和较年长的乳腺癌病例中都可能发现反应性雌激素水平升高,而它们可能表现出雌激素缺乏的临床症状。证明雌激素过多与肿瘤发展之间存在因果关系的研究汇编了这类乳腺癌病例。总之,在乳腺癌病例中对ER难治性进行定量评估非常重要,因为雌激素抵抗力越强,雌激素治疗的希望剂量就越高。

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