微波热疗联合TIPE2可抑制原位结肠癌的生长。

Qingqing Yu, Lingdi Li, Weixing Mo, Linfang Zhao, Lidan Zhang, Ke Zhang, Rongjun Tang
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引用次数: 0

摘要

背景:结肠癌(CC)是人类的主要致命疾病。微波热疗(MH)是多种癌症的辅助疗法。肿瘤坏死因子-α诱导蛋白-8样2(TIPE2)是一种肿瘤抑制因子。然而,MH联合TIPE2对CC的影响仍不清楚:方法:用小鼠CC CT26-Luc细胞构建正位CC小鼠模型,将小鼠随机分为对照组、模型组(CT26-Luc)、CT26-Luc + Vector组、CT26-Luc + TIPE2组、CT26-Luc + MH组和CT26-Luc + MH+TIPE2组(n = 6)。通过体内荧光图像分析检测治疗前和治疗后的肿瘤生长情况。通过 qRT-PCR 和 Western 印迹检测 TIPE2 的表达和细胞转染效率。通过 HE 染色检测病理变化,TUNEL 染色检测细胞凋亡,ELISA 检测血清炎症因子,免疫组化检测 TIPE2 表达,Western 印迹检测 NF-κB 信号转导:结果:癌旁组织的 TIPE2 表达高于 CC 组织。CT26-Luc + TIPE2组、CT26-Luc + MH组和CT26-Luc + MH+TIPE2组减少了肿瘤生长、肿瘤细胞浸润并增加了细胞凋亡。CT26-Luc + TIPE2 组的 NF-κB、TNF-α、IL-1β、IL-6、p-p65 和 p-IKK 表达较低,而 TIPE2 和 IkB 表达升高,CT26-Luc + MH 组则逆转了这一趋势。此外,CT26-Luc+MH+TIPE2组对上述因子表达的影响与CT26-Luc+MH组相反:结论:MH与TIPE2联用可阻碍CC肿瘤的生长,为其在CC治疗中的临床应用提供了科学依据。
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The combination of microwave hyperthermia with TIPE2 impedes the growth of orthotopic colon cancer.

Background: Colon cancer (CC) is the main fatal disease of humans. Microwave hyperthermia (MH) is an adjuvant therapy for diverse cancers. Tumor necrosis factor-α induced protein-8-like 2 (TIPE2) is a tumor suppressor. However, the effect of MH combined with TIPE2 on CC remains unclear.

Methods: The orthotopic CC mouse model was constructed by mouse CC CT26-Luc cells, and mice were randomized into control, model (CT26-Luc), CT26-Luc + Vector, CT26-Luc + TIPE2, CT26-Luc + MH, and CT26-Luc + MH+TIPE2 groups (n = 6). Tumor growth pretreatment and post-treatment by in vivo fluorescence image analysis was detected. TIPE2 expression and cell transfection efficiency was detected by qRT-PCR and western blot. The pathological changes by HE staining, apoptosis by TUNEL staining, serum inflammatory factors by ELISA, TIPE2 expression by immunohistochemistry, and NF-κB signaling by western blot was performed.

Results: Paracancerous tissues showed higher TIPE2 expression than in CC tissues. CT26-Luc + TIPE2, CT26-Luc + MH, and CT26-Luc + MH+TIPE2 groups reduced tumor growth, tumor cell infiltration, and increased apoptosis. CT26-Luc + TIPE2 group had lower NF-κB, TNF-α, IL-1β, IL-6, p-p65, and p-IKK expression, and elevated TIPE2 and IkB expression, which was reversed by CT26-Luc + MH group. Moreover, CT26-Luc+MH+TIPE2 group showed opposite effects on the above factor expression of CT26-Luc+MH group.

Conclusions: Combination of MH with TIPE2 could impede CC tumor growth, providing scientific bases for its clinical application in CC treatment.

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