Knockdown of <scp>RFC</scp>4 inhibits cell proliferation of oral squamous cell carcinoma <i>in vitro</i> and <i>in vivo</i>

Oral squamous cell carcinoma (OSCC) is the one of the most common types of malignant tumor found in the head and neck area. Replication factor C subunit 4 (RFC4), an oncogene active in various human cancers, has been rarely studied in OSCC. In the present study, bioinformatics analysis identified RFC4 as a potential key target in OSCC progression. Additional experiments showed that RFC4 expression was significantly higher in OSCC tumor tissues than in normal tissues. Knockdown of RFC4 led to G2/M phase cell cycle arrest and inhibited the proliferation of OSCC cells both in vitro and in vivo. High RFC4 expression in OSCC tumors was linked to increased levels of MET, along with reduced levels of CD274 and CD160. Overall, the present study reveals that RFC4 may play a pivotal role in OSCC tumorigenesis and could serve as a potential predictive marker for the efficacy of immunotherapy.

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Publication Details

Journal
FEBS Open Bio
Published
2024-12-13
DOI
https://doi.org/10.1002/2211-5463.13929
Citations
4
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.94

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article

Knockdown of RFC4 inhibits cell proliferation of oral squamous cell carcinoma in vitro and in vivo

Ning Xiao, Shuzhen Guan, Zheng Liu, Di Wang et al.
4 citations
FEBS Open Bio
RNA modifications and cancer
0.94
article

Knockdown of RFC4 inhibits cell proliferation of oral squamous cell carcinoma in vitro and in vivo

Ning Xiao, Shuzhen Guan, Zheng Liu, Di Wang, Haotian Chen, Lichuan Wu, Guizhen Wang, Haitao Dong, Pengyue You, Xin Zhang
article en
4 citations

Abstract

Oral squamous cell carcinoma (OSCC) is the one of the most common types of malignant tumor found in the head and neck area. Replication factor C subunit 4 (RFC4), an oncogene active in various human cancers, has been rarely studied in OSCC. In the present study, bioinformatics analysis identified RFC4 as a potential key target in OSCC progression. Additional experiments showed that RFC4 expression was significantly higher in OSCC tumor tissues than in normal tissues. Knockdown of RFC4 led to G2/M phase cell cycle arrest and inhibited the proliferation of OSCC cells both in vitro and in vivo. High RFC4 expression in OSCC tumors was linked to increased levels of MET, along with reduced levels of CD274 and CD160. Overall, the present study reveals that RFC4 may play a pivotal role in OSCC tumorigenesis and could serve as a potential predictive marker for the efficacy of immunotherapy.

FEBS Open BioVol. 15(2)
Guangxi University (CN), Guangxi Medical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking Union Medical College Hospital (CN)
National Natural Science Foundation of China, Peking Union Medical College Hospital, Peking Union Medical College, Fundamental Research Funds for the Central Universities
Good health and well-being
Openalex Percentile: Top 24%
RNA modifications and cancer
0.94
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Knockdown of <scp>RFC</scp>4 inhibits cell proliferation of oral squamous cell carcinoma <i>in vitro</i> and <i>in vivo</i> — Ning Xiao, Shuzhen Guan, et al. · FEBS Open Bio (2024) | TGRS Research Map | TGRS