Brocco Davide, Florio Rosalba, De Lellis Laura, Veschi Serena, Grassadonia Antonino, Tinari Nicola, Cama Alessandro
Department of Pharmacy, "G. d'Annunzio" University of Chieti-Pescara, Via Dei Vestini 31, 66100 Chieti, Italy.
Department of Medical, Oral and Biotechnological Sciences, University "G. d'Annunzio", Chieti-Pescara, 66100 Chieti, Italy.
Cancers (Basel). 2020 Jul 9;12(7):1849. doi: 10.3390/cancers12071849.
Pancreatic cancer (PC) is a lethal malignancy with rising incidence and limited therapeutic options. Obesity is a well-established risk factor for PC development. Moreover, it negatively affects outcome in PC patients. Excessive fat accumulation in obese, over- and normal-weight individuals induces metabolic and inflammatory changes of adipose tissue microenvironment leading to a dysfunctional adipose "organ". This may drive the association between abnormal fat accumulation and pancreatic cancer. In this review, we describe several molecular mechanisms that underpin this association at both local and systemic levels. We focus on the role of adipose tissue-derived circulating factors including adipokines, hormones and pro-inflammatory cytokines, as well as on the impact of the local adipose tissue in promoting PC. A discussion on potential therapeutic interventions, interfering with pro-tumorigenic effects of dysfunctional adipose tissue in PC, is included. Considering the raise of global obesity, research efforts to uncover the molecular basis of the relationship between pancreatic cancer and adipose tissue dysfunction may provide novel insights for the prevention of this deadly disease. In addition, these efforts may uncover novel targets for personalized interventional strategies aimed at improving the currently unsatisfactory PC therapeutic options.
胰腺癌(PC)是一种致命的恶性肿瘤,其发病率不断上升且治疗选择有限。肥胖是PC发生的一个公认的危险因素。此外,它对PC患者的预后产生负面影响。肥胖、超重和正常体重个体体内过多的脂肪堆积会引起脂肪组织微环境的代谢和炎症变化,导致脂肪“器官”功能失调。这可能促使异常脂肪堆积与胰腺癌之间产生关联。在本综述中,我们描述了在局部和全身水平上支撑这种关联的几种分子机制。我们重点关注脂肪组织衍生的循环因子的作用,包括脂肪因子、激素和促炎细胞因子,以及局部脂肪组织在促进PC方面的影响。还包括对潜在治疗干预措施的讨论,这些干预措施可干扰功能失调的脂肪组织在PC中的促肿瘤作用。鉴于全球肥胖率的上升,揭示胰腺癌与脂肪组织功能障碍之间关系的分子基础的研究工作可能为预防这种致命疾病提供新的见解。此外,这些努力可能会发现新的靶点,用于制定个性化的干预策略,以改善目前不尽人意的PC治疗选择。