Growth hormone and radiation therapy: friend, foe, or both?

Endocrine-related cancer Pub Date : 2024-01-24 Print Date: 2024-03-01 DOI:10.1530/ERC-22-0371
Verónica A Bahamondes Lorca, Shiyong Wu
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Abstract

Radiotherapy is one of the major options currently for cancer treatment. Radiotherapy causes cellular damage inducing cell death, which is expected to be selective for tumor cells. However, side effects that alter the surrounding normal tissue are often hard to be avoided. When radiation involves the hypothalamic-pituitary axis, growth hormone deficiency (GHD) is frequently induced, causing developmental and metabolic-related diseases in childhood cancer survivors. Growth hormone (GH) replacement therapy has been used for these patients and has been shown to be safe in general. However, there are some debating for its long-term safety due to the known roles of GH in inducing cell growth, which could be related to cancer recurrence. In addition, studies have shown that GH is involved in the development of resistance to chemotherapy and radiotherapy through various mechanisms. In this review, we will first discuss the effects of GHD induced after radiotherapy and the safety of the GH replacement treatment. Then, we will discuss the role of the GH-IGF-1 axis in radioresistance via a mechanism of improving DNA repair.

生长激素和放射治疗:朋友、敌人,还是两者兼而有之?
放疗是目前治疗癌症的主要方法之一。放疗会造成细胞损伤,诱导细胞死亡,对肿瘤细胞具有选择性。然而,改变周围正常组织的副作用往往难以避免。当放射线涉及下丘脑-垂体轴时,经常会诱发生长激素缺乏症(GHD),导致儿童癌症幸存者出现发育和代谢相关疾病。生长激素(GH)替代疗法已被用于这些患者,并被证明总体上是安全的。然而,由于已知生长激素具有诱导细胞生长的作用,可能与癌症复发有关,因此对其长期安全性存在争议。此外,研究还表明 GH 通过各种机制参与化疗和放疗耐药性的形成。在这篇综述中,我们将首先讨论放疗后诱发 GHD 的影响,以及 GH 替代治疗的安全性。然后,我们将讨论 GH-IGF-1 轴通过改善 DNA 修复机制在放射抗性中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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