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KHDRBS3 promotes multi‐drug resistance and anchorage‐independent growth in colorectal cancer

机译:KHDRBS3促进了结直肠癌中的多药物抵抗和锚固无关的生长

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摘要

5‐Fluorouracil (5‐FU) is one of the most frequently used pharmacological agents in the treatment of colorectal cancer (CRC). Resistance to chemotherapy is a major cause of treatment failure of CRC, and it is a well known fact that cancer stem cells play a significant role in the acquisition of drug resistance. In this study, we focused on the KHDRBS3 gene that encodes KH RNA Binding Domain Containing, Signal Transduction Associated 3. We first clarified the relationship between KHDRBS3 and 5‐FU resistance. We then observed higher expression levels of KHDRBS3 in KRAS‐mutant organoids and cell lines in comparison with KRAS wild‐type organoids and cell lines. Immunohistochemical analysis using CRC cases revealed that the prognosis of KHDRBS3‐positive patients was significantly worse compared with that of KHDRBS3‐negative patients. Univariate and multivariate Cox proportional hazards analyses showed that KHDRBS3 was an independent prognostic factor in patients with CRC. We determined that KHDRBS3 might play a crucial role in the acquisition of stem cell properties, such as drug resistance and spheroid/organoid formation, by regulating CD44 variant expression and the Wnt signaling pathway. In an immunodeficient mouse model, KHDRBS3‐positive cells showed efficient tumor formation and formed metastatic lesions in the lungs. These results indicated that KHDRBS3 plays a crucial role in drug resistance and anchorage‐independent growth by maintaining stem cell‐like features in CRC cells. KHDRBS3 could be a promising candidate marker for predicting chemotherapeutic effect and prognosis in CRC patients.
机译:5-氟尿嘧啶(5-FU)是治疗结肠直肠癌(CRC)中最常用的药理学剂之一。抗化疗是CRC治疗失败的主要原因,众所周知的事实是癌症干细胞在获取耐药性中发挥着重要作用。在本研究中,我们专注于编码含KH RNA结合结构域的KHDRBS3基因,信号转导相关3.我们首先阐明了KHDRBS3和5-FU抗性之间的关系。然后,与KRAS野生型有机体和细胞系相比,我们观察到KRAS-突变有机体和细胞系中KHDRBS3的更高表达水平。使用CRC病例的免疫组织化学分析表明,与KHDRBS3阴性患者的KHDRBS3阳性患者的预后显着差。单变量和多元COX比例危害分析表明,KHDRBS3是CRC患者的独立预后因素。我们通过调节CD44变体表达和WNT信号通路,KHDRBS3在获取干细胞性质(例如耐药性和球形/有机体形成)中可能发挥至关重要的作用。在免疫缺陷小鼠模型中,KHDRBS3阳性细胞显示出高效的肿瘤形成和肺部形成的转移性病变。这些结果表明,KHDRBS3通过在CRC细胞中维持干细胞样特征来对耐药性和锚固无关的生长起着至关重要的作用。 KHDRBS3可能是一个有希望的候选标志物,用于预测CRC患者的化学治疗效果和预后。

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