1.The role of hypoxia-induced circ_0007766 expression in the proliferation, migration and invasion of PCa cells
ZHAO Ziqi1 ; ZHANG Min1 ; YANG Tao1 ; YANG Li2 ; LIAO Guoling1 ; ZHANG Wei1 ; CHU Yuankui1,3
Chinese Journal of Cancer Biotherapy 2025;32(5):460-468
[摘 要] 目的:探讨环化自erb-b2受体酪氨酸激酶2(ERBB2)基因的circ_0007766分子在前列腺癌(PCa)细胞中的作用及缺氧对其表达调控的影响。方法:qRT-PCR检测circ_0007766分子在PCa细胞及组织中的表达;分别转染circ0007766的siRNA至PCa细胞DU145和PC3中,平板克隆实验、CCK-8实验和Transwell 实验检测circ_0007766敲低对PCa细胞克隆形成、增殖、迁移和侵袭能力的影响;厌氧袋法建立DU145和PC3细胞的缺氧细胞模型,WB法检测缺氧通路关键分子HIF-1α的蛋白表达,qRT-PCR检测缺氧模型细胞中circ_0007766分子的表达,WB检测RNA结合蛋白真核翻译起始因子4A3(EIF4A3)的蛋白水平表达,RNA免疫沉淀(RIP)法检测缺氧条件下EIF4A3与circ_0007766的结合,qRT-PCR进一步检测缺氧条件下敲低EIF4A3对circ_0007766表达的影响。结果:circ_0007766在PCa细胞(P < 0.01)及PCa组织(P < 0.05)中呈高表达;敲低circ_0007766(P < 0.05或P < 0.01)能显著抑制PCa细胞的增殖、迁移和侵袭能力(均P < 0.01)。缺氧条件下HIF-1α蛋白表达增加,表明缺氧细胞模型建立成功。qRT-PCR检测结果显示,相较于常氧组,缺氧组circ_0007766的表达显著升高(P < 0.01),WB法检测结果显示缺氧组细胞中EIF4A3 的蛋白表达增强。RIP实验结果显示,circ_0007766在EIF4A3富集组高度富集(P < 0.01)。qRT-PCR检测结果显示,缺氧可显著促进circ_0007766的表达,同时,敲低EIF4A3分子可显著降低缺氧诱导的circ_0007766的表达(P < 0.05或P < 0.01)。结论: circ_0007766在PCa细胞中扮演着促癌分子的角色,其表达形成与缺氧条件下EIF4A3分子的调控有关。
2.Effects and mechanisms of lncRNA PTENP1 on proliferation, apoptosis, migration, and invasion of bladder cancer cells by regulating SCARA5 expression
WANG Jing1 ; SUN Ying1 ; ZHOU Min1 ; ZHAO Qibo1 ; YANG Meng2 ; HUANG Ziming3
Chinese Journal of Cancer Biotherapy 2025;32(11):1151-1158
[摘 要] 目的:探究骨髓间充质干细胞(BMSC)衍生的外泌体lncRNA PTENP1在膀胱癌进展中的功能机制。方法:采用透射电子显微镜、纳米颗粒追踪分析及WB法检测外泌体标志蛋白的方式鉴定BMSC来源的外泌体(BMSC-Exo)。通过共聚焦显微镜检测 BMSC-Exo被膀胱癌5637细胞内化的过程。按转染物不同,将膀胱癌5637和T24细胞随机分为以下组别:对照组、BMSC-Exo组、BMSC OE-NC-Exo组、BMSC OE-PTENP1-Exo组、BMSC sh-NC-Exo组和BMSC sh-PTENP1-Exo组。采用CCK-8、集落形成实验评估细胞增殖水平,流式细胞术评估细胞凋亡水平,划痕愈合和Transwell实验评估细胞迁移和侵袭能力。通过RNA下拉(Pull down)、RNA免疫沉淀(RIP)技术验证miR-17和PTENP1、A类清道夫受体5型(SCARA5)mRNA之间的靶向结合关系。结果:qRT-PCR显示过表达PTENP1的BMSC外泌体(BMSC OE-PTENP1-Exo)显著提升膀胱癌细胞中PTENP1水平(P < 0.01)。BMSC OE-PTENP1-Exo抑制细胞增殖(P < 0.01)、迁移(P < 0.01)和侵袭(P < 0.01),促进细胞凋亡(P < 0.01)。此外,体内实验显示BMSC OE-PTENP1-Exo显著抑制裸鼠移植瘤生长(P < 0.01)。结论:BMS-Exo可通过递送PTENP1作为miR-17的“分子海绵”,解除miR-17对SCARA5的抑制作用,进而上调SCARA5的表达,抑制膀胱癌细胞的恶性生物学行为。
3.Barrier materials for postoperative abdonimal adhesion: biological characteristics,merits and demerits
Lili1,2 YANG ; Yaoyao3 BIAN ; Min1 ZHAO ; Yetong3 WANG ; Shengjin3 TANG ; Wenlin2 LI ; Li1,2 ZENG
Chinese Journal of Tissue Engineering Research 2019;23(2):272-277
BACKGROUND: Postoperative abdominal adhesion is one of the most urgent surgical problems. In view of the complicated pathological mechanisms and various risk factors of postoperative adhesion, surgical techniques and barrier materials have increasingly become the focus of postoperative prevention of adhesion. OBJECTIVE: To summarize the pathological mechanisms and risk factors of postoperative abdominal adhesions and to review the material source, biological characteristics, current research status, and potential deficiencies of different types of barrier materials. METHODS: We retrieved PubMed, CNKI, WanFang and VIP databases from their inception dates to January 2018, and "postoperative abdominal adhesion, etiology and pathogenesis, risk factors, preventive measures, barrier materials" were used as the keywords in English and Chinese, respectively. Fifty-four articles were included in final analysis. RESULTS AND CONCLUSION: Anti-adhesion materials can isolate the injured area and peripheral tissues through physical barriers in the early stage of adhesion formation, and thus prevent the formation of abdominal adhesion. There are three types of anti-adhesion barrier material at present, including solution, gel and membrane agents. Each kind of material has its own advantages and disadvantages. Therefore we explore the pathological process of postoperative abdominal adhesions, predict the risk factors of postoperative adhesions, improve surgical skills and select appropriate anti-adhesion barrier materials according to actual conditions, which are expected to reduce the formation of postoperative abdominal adhesions.

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