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IGF-II Producing Hepatocellular Carcinoma Treated with Sorafenib: Metabolic Complications and a Foresight to Molecular Targeting Therapy to the IGF Signal

机译:索拉非尼治疗IGF-II产生的肝细胞癌:代谢并发症和对IGF信号分子靶向治疗的远见。

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摘要

Hypoglycemia is a rare paraneoplastic manifestation of patients with neoplasms. Hypoglycemia can be induced by several causes, including an aberrant increase of hypoglycemic agents and adrenal insufficiency. Sorafenib is the first agent to demonstrate a survival benefit in the treatment of advanced hepatocellular carcinoma (HCC). This small molecule inhibits serine/threonine kinase RAF in tumor cells and tyrosine kinases VEGFR/PDGFR in tumor vasculature and decreases tumor growth and angiogenesis. In this paper, we report a case of HCC who was treated with sorafenib and showed severe hypoglycemia. This hypoglycemia might be induced by two causes, both adrenal insufficiency as an adverse effect of sorafenib and activation of the insulin-like growth factor (IGF) signal by excessive secretion of incompletely processed precursors of IGF-II. Although the IGF signal is suggested to be involved in aberrant growth of HCC in some cases, there is no other report showing the influence of sorafenib on HCC with active IGF signal. Unfortunately, the effect of sorafenib was limited in the present case. However, emerging drugs that directly inhibit the IGF signal can be expected to be highly effective in the treatment of HCC with hypoglycemia.
机译:低血糖症是肿瘤患者罕见的副肿瘤表现。低血糖症可由多种原因引起,包括降血糖药异常增加和肾上腺功能不全。索拉非尼是第一种在晚期肝细胞癌(HCC)的治疗中显示生存获益的药物。这个小分子抑制肿瘤细胞中的丝氨酸/苏氨酸激酶RAF和肿瘤血管中的酪氨酸激酶VEGFR / PDGFR,并减少肿瘤的生长和血管生成。在本文中,我们报告了一名接受索拉非尼治疗并显示严重低血糖的肝癌病例。这种低血糖可能是由两种原因引起的,一种是肾上腺功能不全(索拉非尼的不良反应),另一种是由于未完全加工的IGF-II前体的过度分泌而激活了胰岛素样生长因子(IGF)信号。尽管在某些情况下建议IGF信号参与肝癌的异常生长,但尚无其他报道显示索拉非尼对具有活跃IGF信号的肝癌的影响。不幸的是,在本案中索拉非尼的作用有限。但是,可以预期直接抑制IGF信号的新兴药物在治疗低血糖HCC中非常有效。

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