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长链非编码RNA的过表达适用于溶瘤腺病毒H101治疗口腔鳞状细胞癌。

Overexpression of LncRNA Were Suitable for Oncolytic Adenoviruse H101 Therapy in Oral Squamous-Cell Carcinoma.

作者信息

Wang Xin, Yang Song, Lv Xuechao, Wang Lina, Li Chunmei

机构信息

Department of Plastic Maxillofacial Surgery, Heilongjiang Provincial Hospital, Harbin 150036, Heilongjiang, People's Republic of China.

Department of Pediatric Dentistry, School of Stomatology, Harbin Medical University, Harbin 150001, Heilongjiang, People's Republic of China.

出版信息

Onco Targets Ther. 2020 Dec 21;13:13033-13039. doi: 10.2147/OTT.S285536. eCollection 2020.

Abstract

BACKGROUND

As the most prevalent type of head and neck cancer, oral squamous-cell carcinoma (OSCC) accounts for nearly 90% of all oral cancer cases. Despite great progress having been made in the diagnosis and treatment of OSCC recently, the survival rate of OSCC patients has not risen remarkably. Chemotherapy is commonly used for OSCC treatment; however, the emergence of chemoresistance limits its long-term curative effect. Therefore, identifying effective biomarkers and molecular mechanisms is essential to the development of therapeutic strategies for OSCC.

METHODS

qRT-PCR assays were performed to detect expression in OSCC tissue and cells, and CCK8 assays and animal experiments used to examine cell proliferation. In addition, CCK8 assays were used to detect IC values of cisplatin, 5Fu, Dox, and oncolytic adenovirus H101.

RESULTS

We found that was overexpressed in OSCC tissue and cells and was associated with OSCC progression. In addition, knockdown of suppressed cell proliferation in vitro and in vivo. Importantly, we found that oncolytic adenovirus H101 showed better antitumor effects in OSCC with high expression, and chemotherapy showed worse anti-tumor effects in OSCC with high expression.

CONCLUSION

can act as a diagnostic biomarker for OSCC, and may be a biomarker for treatment options.

摘要

背景

作为头颈癌最常见的类型,口腔鳞状细胞癌(OSCC)占所有口腔癌病例的近90%。尽管近年来OSCC的诊断和治疗取得了很大进展,但OSCC患者的生存率并未显著提高。化疗常用于OSCC治疗;然而,化疗耐药性的出现限制了其长期疗效。因此,确定有效的生物标志物和分子机制对于OSCC治疗策略的开发至关重要。

方法

进行qRT-PCR检测OSCC组织和细胞中的表达,并使用CCK8检测和动物实验来检测细胞增殖。此外,使用CCK8检测来检测顺铂、5Fu、阿霉素和溶瘤腺病毒H101的IC值。

结果

我们发现,在OSCC组织和细胞中过表达,且与OSCC进展相关。此外,敲低 在体外和体内均抑制细胞增殖。重要的是,我们发现溶瘤腺病毒H101在高 表达的OSCC中显示出更好的抗肿瘤作用,而化疗在高 表达的OSCC中显示出较差的抗肿瘤作用。

结论

可作为OSCC的诊断生物标志物,并且可能是治疗选择的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9573/7762447/24a509182fbc/OTT-13-13033-g0001.jpg

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