The regulation of long non-coding RNA 00958 (LINC00958) for oral squamous cell carcinoma (OSCC) cells death through absent in melanoma 2 (AIM2) depending on microRNA-4306 and Sirtuin1 (SIRT1) in vitro-Reference-Cited by-同舟云学术

The regulation of long non-coding RNA 00958 (LINC00958) for oral squamous cell carcinoma (OSCC) cells death through absent in melanoma 2 (AIM2) depending on microRNA-4306 and Sirtuin1 (SIRT1) in vitro

Published:2021-01-01 Issue:1 Volume:12 Page:5085-5098
ISSN:2165-5979
Container-title:Bioengineered
language:en
Short-container-title:Bioengineered

Author:

Jiang Lei¹,Ge Wenyu²,Cui Yifei³,Wang Xiaofeng⁴

Affiliation:

1. Department of Pathology, The Second Affiliated Hospital of Harbin Medical University, Heilongjiang. China

2. Department of Stomatology, The Second Affiliated Hospital of Harbin Medical University. Harbin Institute of Technology, Heilongjiang Provincial Hospital, Heilongjiang, China

3. Department of Pathology, Harbin Medical University Cancer Hospital, Heilongjiang, China

4. Department of Stomatology, The Second Affiliated Hospital of Harbin Medical University, Heilongjiang, China

Funder

The study was approved by Natural Science Foundation of Heilongjiang Province

Publisher

Informa UK Limited

Subject

Applied Microbiology and Biotechnology,General Medicine,Bioengineering,Biotechnology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21655979.2021.1955561

Reference42 articles.

1. Collagen Triple Helix Repeat Containing-1 (CTHRC1) Expression in Oral Squamous Cell Carcinoma (OSCC): Prognostic Value and Clinico-Pathological Implications

2. Stromal features are predictive of disease mortality in oral cancer patients

3. A long noncoding RNA critically regulates Bcr-Abl-mediated cellular transformation by acting as a competitive endogenous RNA

4. MicroRNA-487a-3p inhibits the growth and invasiveness of oral squamous cell carcinoma by targeting PPM1A

5. MiR-132 inhibits migration and invasion and increases chemosensitivity of cisplatin-resistant oral squamous cell carcinoma cells via targeting TGF-β1

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