Evidence map›Paper›PMID 36941595›Full record

ArticleBMC cancer2023

TUBA1C: a new potential target of LncRNA EGFR-AS1 promotes gastric cancer progression.

Haodong Wang, Huaiping Cui, Xinjun Yang, Lipan Peng

Open access · goldFull text read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Haodong WangShandong Provincial Hospital Affiliated to Shandong First Medical University, 250000, Jinan, Jinan, China.
Huaiping CuiShandong Provincial Hospital Affiliated to Shandong First Medical University, 250000, Jinan, Jinan, China.
Xinjun YangShandong Provincial Hospital Affiliated to Shandong First Medical University, 250000, Jinan, Jinan, China.
Lipan PengShandong Provincial Hospital Affiliated to Shandong First Medical University, 250000, Jinan, Jinan, China. plp1983@126.com.
Shandong First Medical University · CNShandong Provincial Hospital · CN

Funding

Focus on research and development plan in Shandong province, China 2017GSF221003The Key Research and Development Program of Shandong Province 2019GSF108146
6 · The paper itself

Abstract

backgroundThe lack of obvious symptoms of early gastric cancer (GC) as well as the absence of sensitive and specific biomarkers results in poor clinical outcomes. Tubulin is currently emerging as important regulators of the microtubule cytoskeleton and thus have a strong potential to be implicated in a number of disorders, however, its mechanism of action in gastric cancer is still unclear. Tubulin alpha-1 C (TUBA1C) is a subtype of α-tubulin, high TUBA1C expression has been shown to be closely related to a poor prognosis in various cancers, this study, for the first time, revealed the mechanism of TUBA1C promotes malignant progression of gastric cancer in vitro and in vivo.

methodsThe expression of lncRNA EGFR-AS1 was detected in human GC cell lines by qRT-PCR. Mass spectrometry experiments following RNA pulldown assays found that EGFR-AS1 directly binds to TUBA1C, the CCK8, EdU, transwell, wound-healing, cell cycle assays and animal experiments were conducted to investigate the function of TUBA1C in GC. Combined with bioinformatics analyses, reveal interaction between Ki-67, E2F1, PCNA and TUBA1C by western blot. Rescue experiments furtherly demonstrated the relationship of EGFR-AS1and TUBA1C.

resultsTUBA1C was proved to be a direct target of EGFR-AS1, and TUBA1C promotes gastric cancer proliferation, migration and invasion by accelerating the progression of the cell cycle from the G1 phase to the S phase and activating the expression of oncogenes: Ki-67, E2F1 and PCNA.

conclusionTUBA1C is a new potential target of LncRNA EGFR-AS1 promotes gastric cancer progression and could be a novel biomarker and therapeutic target for GC.

Indexed as

RNA, Long NoncodingStomach NeoplasmsTubulinAnimalsCell Line, TumorCell MovementCell ProliferationErbB ReceptorsGene Expression Regulation, NeoplasticHumansKi-67 AntigenNeoplastic ProcessesPrognosisProliferating Cell Nuclear AntigenEGFR protein, humanErbB ReceptorsKi-67 AntigenProliferating Cell Nuclear AntigenRNA, Long NoncodingTubulinCell cycleGastric cancerLncRNA EGFR-AS1TUBA1C

Identifiers

PMID36941595
PMCPMC10026485
OpenAlexW4328048030

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Textfull text, public
LicenceCC BY
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Read underepoch 390

Registered trials

None linked

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.