Sanchis-Pascual David, Del Olmo-García María Isabel, Prado-Wohlwend Stefan, Zac-Romero Carlos, Segura Huerta Ángel, Hernández-Gil Javier, Martí-Bonmatí Luis, Merino-Torres Juan Francisco
Endocrinology and Nutrition Department, University and Politecnic Hospital La Fe (Valencia), 46026 Valencia, Spain.
Joint Research Unit on Endocrinology, Nutrition and Clinical Dietetics, Health Research Institute La Fe, 46026 Valencia, Spain.
Cancers (Basel). 2024 May 8;16(10):1799. doi: 10.3390/cancers16101799.
There are several well-described molecular mechanisms that influence cell growth and are related to the development of cancer. Chemokines constitute a fundamental element that is not only involved in local growth but also affects angiogenesis, tumor spread, and metastatic disease. Among them, the C-X-C motif chemokine ligand 12 (CXCL12) and its specific receptor the chemokine C-X-C motif receptor 4 (CXCR4) have been widely studied. The overexpression in cell membranes of CXCR4 has been shown to be associated with the development of different kinds of histological malignancies, such as adenocarcinomas, epidermoid carcinomas, mesenchymal tumors, or neuroendocrine neoplasms (NENs). The molecular synapsis between CXCL12 and CXCR4 leads to the interaction of G proteins and the activation of different intracellular signaling pathways in both gastroenteropancreatic (GEP) and bronchopulmonary (BP) NENs, conferring greater capacity for locoregional aggressiveness, the epithelial-mesenchymal transition (EMT), and the appearance of metastases. Therefore, it has been hypothesized as to how to design tools that target this receptor. The aim of this review is to focus on current knowledge of the relationship between CXCR4 and NENs, with a special emphasis on diagnostic and therapeutic molecular targets.
有几种已被充分描述的分子机制会影响细胞生长,且与癌症的发展相关。趋化因子是一个基本要素,不仅参与局部生长,还会影响血管生成、肿瘤扩散和转移性疾病。其中,C-X-C基序趋化因子配体12(CXCL12)及其特异性受体趋化因子C-X-C基序受体4(CXCR4)已得到广泛研究。CXCR4在细胞膜上的过度表达已被证明与不同类型的组织学恶性肿瘤的发展有关,如腺癌、表皮样癌、间充质肿瘤或神经内分泌肿瘤(NENs)。CXCL12与CXCR4之间的分子突触导致G蛋白相互作用以及胃肠胰(GEP)和支气管肺(BP)NENs中不同细胞内信号通路的激活,赋予更大的局部侵袭能力、上皮-间质转化(EMT)和转移的出现。因此,人们一直在设想如何设计针对该受体的工具。本综述的目的是聚焦于CXCR4与NENs之间关系的当前知识,特别强调诊断和治疗分子靶点。