Role of INPP4B in the proliferation, migration, invasion, and survival of human endometrial cancer cells.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-09-01 Epub Date: 2024-01-16 DOI:10.14670/HH-18-711
Jing Zhao, Xue-Mei Du, Wen Si, Xian-He Zhao, Zi-Qi Zhou
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引用次数: 0

Abstract

Background: Inositol polyphosphate 4-phosphatase type II (INPP4B) has been identified as a tumor repressor in several human cancers while its role in endometrial cancer has not been investigated yet. Therefore, the current study was designed to determine whether INPP4B participates in the progression of endometrial cancer by utilizing clinical data and experimental determination.

Materials and methods: We first include six chemotherapy-treated patients with recurrent and metastatic endometrioid carcinoma to determine the relationship between INPP4B mutation and relative tumor burden. By using siRNA-mediated gene silencing and vector-mediated gene overexpression, we further determined the effect of manipulating INPP4B expression on the proliferation, invasion, and survival of endometrial cancer cells. Furthermore, the repressing effect of INPP4B together with its role in chemotherapy was further validated by xenograft tumor-bearing mice models. Western blot analysis was used to explore further downstream signaling modulated by INPP4B expression manipulation.

Results: Two of the patients were found to have INPP4B mutations and the mutation frequency of INPP4B increased during the progression of chemotherapy resistance. Endometrial cancer cells with silenced INPP4B expression were found to have promoted tumor cell proliferation, invasion, and survival. Endometrial cancer cells overexpressing INPP4B were found to have decreased tumor cell proliferation, invasion, and survival. An in vivo study using six xenograft tumor-bearing mice in each group revealed that INPP4B overexpression could suppress tumor progression and enhance chemosensitivity. Furthermore, INPP4B overexpression was found to modulate the activation of Wnt3a signaling.

Conclusion: The current study suggested that INPP4B could be a suppressor in endometrial cancer progression and might be a target for endometrial cancer treatment. Also, INPP4B might serve as a predictor of chemosensitivity determination.

INPP4B 在人类子宫内膜癌细胞的增殖、迁移、侵袭和存活中的作用。
背景:肌醇多磷酸4-磷酸酶II型(INPP4B)已被确认为多种人类癌症的肿瘤抑制因子,但其在子宫内膜癌中的作用尚未得到研究。因此,本研究旨在通过临床数据和实验测定来确定 INPP4B 是否参与了子宫内膜癌的进展:我们首先纳入了六名化疗后的复发性和转移性子宫内膜样癌患者,以确定 INPP4B 突变与相对肿瘤负荷之间的关系。通过 siRNA 介导的基因沉默和载体介导的基因过表达,我们进一步确定了操纵 INPP4B 表达对子宫内膜癌细胞增殖、侵袭和存活的影响。此外,我们还通过异种移植肿瘤小鼠模型进一步验证了 INPP4B 的抑制作用及其在化疗中的作用。研究人员还利用 Western 印迹分析进一步探讨了 INPP4B 表达调控对下游信号传导的影响:结果:发现其中两名患者存在 INPP4B 基因突变,且在化疗耐药进展过程中 INPP4B 基因突变频率增加。沉默 INPP4B 表达的子宫内膜癌细胞可促进肿瘤细胞的增殖、侵袭和存活。研究发现,过表达 INPP4B 的子宫内膜癌细胞会减少肿瘤细胞的增殖、侵袭和存活。一项使用每组六只异种移植肿瘤小鼠进行的体内研究显示,INPP4B 过表达可抑制肿瘤进展并增强化疗敏感性。此外,研究还发现 INPP4B 的过表达可调节 Wnt3a 信号的激活:本研究表明,INPP4B 可能是子宫内膜癌进展的抑制因子,并可能成为子宫内膜癌治疗的靶点。结论:本研究表明,INPP4B可能是子宫内膜癌进展的抑制因子,也可能是子宫内膜癌治疗的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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