Evidence map›Paper›PMID 33658048›Full record

ArticleCancer cell international2021

LINC00958 promotes the proliferation of TSCC via miR-211-5p/CENPK axis and activating the JAK/STAT3 signaling pathway.

Bo Jia, Junfeng Dao, Jiusong Han, Zhijie Huang, Xiang Sun, Xianghuai Zheng, Shijian Xiang, Huixi Zhou, Shuguang Liu

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 36 citations in OpenAlex.

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  11. Centromeric protein K (CENPK) promotes gastric cancer proliferation and migration via interacting with XRCC5.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Bo Jia *Department of Stomatology, Shunde Hospital, Southern Medical University, Foshan, Guangdong, 528300, China.
Junfeng Dao *Department of Prosthodontics, Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China.
Jiusong HanDepartment of Oral Surgery, Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China.
Zhijie HuangDepartment of Oral Surgery, Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China.
Xiang SunDepartment of Oral Surgery, Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China.
Xianghuai ZhengDepartment of Oral Surgery, Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China.
Shijian XiangDepartment of Pharmacy, Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, 518107, China.
Huixi ZhouDepartment of Oral Surgery, Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China. zhouhuixikqwk@163.com.
Shuguang LiuDepartment of Oral Surgery, Stomatological Hospital, Southern Medical University, Guangzhou, 510280, China. liushuguangwk@163.com.ORCID http://orcid.org/0000-0003-0066-1020
Southern Medical University · CNSun Yat-sen University · CNThe First People's Hospital of Shunde · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTongue squamous cell carcinoma (TSCC) is one of the most common oral tumors. Recently, long intergenic noncoding RNA 00958 (LINC00958) has been identified as an oncogene in human cancers. Nevertheless, the role of LINC00958 and its downstream mechanisms in TSCC is still unknown.

methodsThe effect of LINC00958 on TSCC cells proliferation and growth were assessed by CCK-8, colony formation, 5-Ethynyl-2'-deoxyuridline (EdU) assay and flow cytometry assays in vitro and tumor xenograft model in vivo. Bioinformatics analysis was used to predict the target of LINC00958 in TSCC, which was verified by RNA immunoprecipitation and luciferase reporter assays.

resultsLINC00958 was increased in TSCC tissues, and patients with high LINC00958 expression had a shorter overall survival. LINC00958 knockdown significantly decreased the growth rate of TSCC cells both in vitro and in vivo. In mechanism, LINC00958 acted as a ceRNA by competitively sponging miR-211-5p. In addition, we identified CENPK as a direct target gene of miR-211-5p, which was higher in TSCC tissues than that in adjacent normal tissues. Up-regulated miR-211-5p or down-regulated CENPK could abolish LINC00958-induced proliferation promotion in TSCC cells. Furthermore, The overexpression of CENPK promoted the expression of oncogenic cell cycle regulators and activated the JAK/STAT3 signaling.

conclusionsOur findings suggested that LINC00958 is a potential prognostic biomarker in TSCC.

Indexed as

CENPKLINC00958miR-211-5pProliferationTSCC

Identifiers

PMID33658048
PMCPMC7931557
OpenAlexW3126783645

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.