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解析瘦素和脂联素在肥胖相关胃肠癌中的作用。

Decoding the role of leptin and adiponectin in obesity-related gastrointestinal cancer.

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisboa, Portugal.

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.

出版信息

Clin Sci (Lond). 2023 Aug 14;137(15):1095-1114. doi: 10.1042/CS20230411.

Abstract

The increasing prevalence of obesity brings forward its importance as a risk factor for cancer development, particularly in the gastrointestinal tract. Obesity may trigger cancer development through several mechanisms, where metabolic deregulation of adipokines can modulate multiple oncogenic molecular pathways. Leptin and adiponectin are the most well-studied adipokines, and their imbalance can trigger different tumorigenic responses. Both epidemiologic and experimental studies have associated leptin with increased cancer risk and cell responsiveness in carcinogenesis and tumor invasion. On the other hand, adiponectin is reported to elicit the opposite effect. In addition to circulating or tissue adipokine levels, adiponectin, and leptin receptors or genetic polymorphisms may also play a role in cancer development. Moreover, adiponectin and leptin modulation offer valuable therapeutic approaches. We will review the links underpinning obesity and cancer development and focus on discussing the pathophysiological roles of leptin and adiponectin.

摘要

肥胖症的发病率不断上升,使其成为癌症发展的一个重要风险因素,尤其是在胃肠道中。肥胖可能通过多种机制引发癌症的发生,其中脂肪因子的代谢失调可以调节多种致癌分子途径。瘦素和脂联素是研究最多的脂肪因子,它们的失衡会引发不同的肿瘤发生反应。流行病学和实验研究都表明,瘦素与癌症风险的增加以及致癌作用和肿瘤侵袭中的细胞反应性有关。另一方面,有报道称脂联素会产生相反的效果。除了循环或组织脂肪因子水平外,脂联素和瘦素受体或遗传多态性也可能在癌症发展中发挥作用。此外,脂联素和瘦素的调节为提供了有价值的治疗方法。我们将回顾肥胖症与癌症发展之间的联系,并重点讨论瘦素和脂联素的病理生理作用。

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