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微小RNA-135a通过靶向BMI1和KLF4减少骨肉瘤肺转移。

miR-135a Reduces Osteosarcoma Pulmonary Metastasis by Targeting Both BMI1 and KLF4.

作者信息

Chen Chenglong, Mao Xingjia, Cheng Caitong, Jiao Yurui, Zhou Yi, Ren Tingting, Wu Zhuangzhuang, Lv Zhi, Sun Xiaojuan, Guo Wei

机构信息

Musculoskeletal Tumor Center, Peking University People's Hospital, Beijing, China.

Beijing Key Laboratory of Musculoskeletal Tumor, Peking University People's Hospital, Beijing, China.

出版信息

Front Oncol. 2021 Mar 22;11:620295. doi: 10.3389/fonc.2021.620295. eCollection 2021.

Abstract

Because of the modest response rate after surgery and chemotherapy, treatment of osteosarcoma (OS) remains challenging due to tumor recurrence and metastasis. miR-135a has been reported to act as an anticarcinogenic regulator of several cancers. However, its expression and function in osteosarcoma remain largely unknown. Here, we reported that abridged miR-135a expression in OS cells and tissues, and its expression is inversely correlated with the expression of BMI1 and KLF4, which are described as oncogenes in several cancers. Ectopic expression of miR-135a inhibited cell invasion and expression of BMI1 and KLF4 in OS cells. investigation confirmed that miR-135a acts as a tumor suppressor in OS to inhibit tumor growth and lung metastasis in xenograft nude mice. BMI1 and KLF4 were revealed to be direct targets of miR-135a, and miR-135a had a similar effect as the combination of si-BMI1 and si-KLF4 on inhibiting tumor progression and the expression of BMI1 and KLF4 . Altogether, our results demonstrate that the targeting of BMI1/KLF4 with miR-135a may provide an applicable strategy for exploring novel therapeutic approaches for OS.

摘要

由于骨肉瘤(OS)手术后和化疗后的缓解率不高,肿瘤复发和转移使得骨肉瘤的治疗仍然具有挑战性。据报道,miR-135a在多种癌症中作为抗癌调节因子发挥作用。然而,其在骨肉瘤中的表达和功能仍 largely未知。在此,我们报道了miR-135a在OS细胞和组织中的表达缩短,并且其表达与BMI1和KLF4的表达呈负相关,BMI1和KLF4在多种癌症中被描述为癌基因。miR-135a的异位表达抑制了OS细胞的侵袭以及BMI1和KLF4的表达。研究证实,miR-135a在OS中作为肿瘤抑制因子发挥作用,抑制异种移植裸鼠中的肿瘤生长和肺转移。BMI1和KLF4被揭示为miR-!35a的直接靶标,并且miR-135a在抑制肿瘤进展以及BMI1和KLF4的表达方面具有与si-BMI1和si-KLF4组合类似的效果。总之,我们的结果表明,用miR-135a靶向BMI1/KLF4可能为探索骨肉瘤的新型治疗方法提供一种可行的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a0c/8019936/b89512657356/fonc-11-620295-g001.jpg

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