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PFKFB2 通过抑制转移和肿瘤糖酵解成为结直肠癌的有利预后生物标志物。

PFKFB2 is a favorable prognostic biomarker for colorectal cancer by suppressing metastasis and tumor glycolysis.

机构信息

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, 651 Dongfeng Road East, Guangzhou, 510060, China.

Department of Clinical Research, Sun Yat-Sen University Cancer Center, 651 Dongfeng Road East, Guangzhou, 510060, China.

出版信息

J Cancer Res Clin Oncol. 2023 Sep;149(12):10737-10752. doi: 10.1007/s00432-023-04946-1. Epub 2023 Jun 13.

Abstract

PURPOSE

This study was to investigate the biological effect of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 2 (PFKFB2) in colorectal cancer (CRC).

METHODS

PFKFB2 was selected by metabolism polymerase chain reaction (PCR) array from CRC cells under alkaline culture medium (pH 7.4) and acidic culture medium (pH 6.8). The expression of PFKFB2 mRNA and protein was detected by quantitative real-time PCR and immunohistochemistry in 70 paired fresh and 268 paired paraffin-embedded human CRC tissues, respectively, and then the prognostic value of PFKFB2 was investigated. The effects of PFKFB2 on CRC cells were also verified in vitro, which were through detecting the change of migration, invasion, sphere formation, proliferation, colony formation, and extracellular acidification rate of CRC cells after PFKFB2 knockdown in alkaline culture medium (pH 7.4) and overexpression in acidic culture medium (pH 6.8).

RESULTS

PFKFB2 expression was downregulated in acidic culture medium (pH 6.8). In addition, we found PFKFB2 expression decreased in human CRC tissues compared with the adjacent normal tissues. Furthermore, the OS and DFS rate of CRC patients with low PFKFB2 expression was significantly shorter than those of patients with high PFKFB2 expression. Multivariate analysis indicated that low PFKFB2 expression was an independent prognostic factor for both OS and DFS in CRC patients. Moreover, the abilities of migration, invasion, spheroidizing ability, proliferation, and colony formation of CRC cells were significantly increased after depletion of PFKFB2 in alkaline culture medium (pH 7.4) and decreased after overexpression of PFKFB2 in acidic culture medium (pH 6.8) in vitro. Epithelial-mesenchymal transition (EMT) pathway was found and verified involved in the PFKFB2-mediated regulation of metastatic function in CRC cells. Further, glycolysis of CRC cells was significantly elevated after knockdown of PFKFB2 in alkaline culture medium (pH 7.4) and decreased after overexpression of PFKFB2 in acidic culture medium (pH 6.8).

CONCLUSION

PFKFB2 expression is downregulated in CRC tissues and associated with worse survival for CRC patients. PFKFB2 could inhibit metastasis and the malignant progression of CRC cells by suppressing EMT and glycolysis.

摘要

目的

本研究旨在探讨 6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶 2(PFKFB2)在结直肠癌(CRC)中的生物学作用。

方法

采用代谢聚合酶链反应(PCR)阵列从碱性培养条件(pH7.4)和酸性培养条件(pH6.8)下的 CRC 细胞中选择 PFKFB2。通过定量实时 PCR 和免疫组织化学分别检测 70 对新鲜和 268 对石蜡包埋的人 CRC 组织中 PFKFB2mRNA 和蛋白的表达,并进一步研究 PFKFB2 的预后价值。还在体外验证了 PFKFB2 对 CRC 细胞的影响,方法是在碱性培养条件(pH7.4)中敲低 PFKFB2 以及在酸性培养条件(pH6.8)中过表达 PFKFB2 后,检测 CRC 细胞迁移、侵袭、球体形成、增殖、集落形成和细胞外酸化率的变化。

结果

在酸性培养条件(pH6.8)中,PFKFB2 的表达下调。此外,我们发现与相邻正常组织相比,PFKFB2 在人 CRC 组织中的表达降低。此外,PFKFB2 低表达的 CRC 患者的 OS 和 DFS 率明显短于 PFKFB2 高表达的患者。多变量分析表明,PFKFB2 低表达是 CRC 患者 OS 和 DFS 的独立预后因素。此外,在体外碱性培养条件(pH7.4)中敲低 PFKFB2 以及酸性培养条件(pH6.8)中过表达 PFKFB2 后,CRC 细胞的迁移、侵袭、球体形成能力、增殖和集落形成能力均显著增强。上皮-间充质转化(EMT)通路被发现并验证参与了 PFKFB2 对 CRC 细胞转移功能的调节。进一步研究发现,在碱性培养条件(pH7.4)中敲低 PFKFB2 后,CRC 细胞的糖酵解明显升高,而在酸性培养条件(pH6.8)中过表达 PFKFB2 后,糖酵解降低。

结论

PFKFB2 在 CRC 组织中表达下调,并与 CRC 患者的生存预后不良相关。PFKFB2 可通过抑制 EMT 和糖酵解来抑制 CRC 细胞的转移和恶性进展。

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