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莪术烯醇靶向14-3-3γ蛋白抑制磷酸戊糖途径并增强顺铂的抗肿瘤作用

Curcumenol Targeting YWHAG Inhibits the Pentose Phosphate Pathway and Enhances Antitumor Effects of Cisplatin.

作者信息

Mao Zhijie, Zhong Liyan, Zhuang Xiaodan, Liu Haoen, Peng Yan

机构信息

ChangZhou Wujin People's Hospital, Changzhou 213017, Jiangsu, China.

Wujin Hospital Affiliated with Jiangsu University, Changzhou 213017, Jiangsu, China.

出版信息

Evid Based Complement Alternat Med. 2022 Jun 26;2022:3988916. doi: 10.1155/2022/3988916. eCollection 2022.

Abstract

OBJECTIVE

Cervical cancer is a common cancer in women. The drug resistance of chemotherapeutic agents has always been an urgent problem to be solved in clinics. The purpose of this study was to determine the role of tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma polypeptide (YWHAG) in cervical cancer and explore the effect of on cervical cancer and its possible mechanism.

METHODS

YWHAG expression in cervical cancer was confirmed using The Cancer Genome Atlas (TCGA) database. Then, the effects of YWHAG on the proliferation and invasion of HeLa and C33A cervical cancer cells were detected by the cell counting kit-8 (CCK-8) and transwell assay. The relationship between YWHAG and the pentose phosphorylation pathway was further studied. CCK-8, Edu, and quantitative real-time polymerase chain reaction were used to confirm that inhibited the sensitivity of YWHAG to cisplatin chemotherapy and to detect the expression of apoptosis-related proteins.

RESULTS

YWHAG was highly expressed in cervical cancer and was associated with poor prognosis. The proliferation and invasion abilities of HeLa and C33A cells decreased after YWHAG knockout. The TCGA database of cervical cancer showed a positive correlation between YWHAG and hypoxia-inducible factor-1 subunit alpha (HIF-1) expression. YWHAG expression increased with HIF-1 overexpression. YWHAG knockdown reduced the protein expression in the pentose phosphorylation pathway. Curcumenol inhibited YWHAG expression. Compared with cisplatin alone, curcumenol combined with cisplatin can reduce cell proliferation and invasion and reduce matrix metalloproteinase (MMP) 2 and MMP9 expression. It can also increase apoptosis, decrease B cell lymphoma 2 (Bcl-2) expression, and increase the expression of Bcl-2 antagonist X, caspase-3, and polyadenosine diphosphate-ribose polymerase.

CONCLUSION

YWHAG can interact with HIF-1 to affect the proliferation and invasion of cervical cancer cells. YWHAG knockout can reduce the expression of pentose phosphorylation pathway-related proteins. Curcumenol can enhance cisplatin to inhibit cancer cell proliferation, migration, and invasion and promote tumor cell apoptosis. The combination of drugs may promote the apoptosis of cervical cancer cells through the YWHAG pathway.

摘要

目的

宫颈癌是女性常见的癌症。化疗药物的耐药性一直是临床上亟待解决的问题。本研究旨在确定酪氨酸3 - 单加氧酶/色氨酸5 - 单加氧酶激活蛋白γ多肽(YWHAG)在宫颈癌中的作用,探讨其对宫颈癌的影响及其可能机制。

方法

使用癌症基因组图谱(TCGA)数据库确认YWHAG在宫颈癌中的表达。然后,通过细胞计数试剂盒 - 8(CCK - 8)和Transwell实验检测YWHAG对HeLa和C33A宫颈癌细胞增殖和侵袭的影响。进一步研究YWHAG与磷酸戊糖途径的关系。使用CCK - 8、Edu和定量实时聚合酶链反应来确认姜黄烯醇抑制YWHAG对顺铂化疗的敏感性,并检测凋亡相关蛋白的表达。

结果

YWHAG在宫颈癌中高表达,且与预后不良相关。YWHAG基因敲除后,HeLa和C33A细胞的增殖和侵袭能力下降。宫颈癌的TCGA数据库显示YWHAG与缺氧诱导因子 - 1α亚基(HIF - 1)表达呈正相关。随着HIF - 1过表达,YWHAG表达增加。YWHAG敲低降低了磷酸戊糖途径中的蛋白表达。姜黄烯醇抑制YWHAG表达。与单独使用顺铂相比,姜黄烯醇联合顺铂可降低细胞增殖和侵袭,降低基质金属蛋白酶(MMP)2和MMP9表达。它还可增加细胞凋亡,降低B细胞淋巴瘤2(Bcl - 2)表达,并增加Bcl - 2拮抗剂X、半胱天冬酶 - 3和聚腺苷二磷酸 - 核糖聚合酶的表达。

结论

YWHAG可与HIF - 1相互作用,影响宫颈癌细胞的增殖和侵袭。YWHAG基因敲除可降低磷酸戊糖途径相关蛋白的表达。姜黄烯醇可增强顺铂抑制癌细胞增殖、迁移和侵袭的能力,并促进肿瘤细胞凋亡。联合用药可能通过YWHAG途径促进宫颈癌细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4580/9251105/3ec8b4ff0f3e/ECAM2022-3988916.001.jpg

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