Evidence map›Paper›PMID 36175877›Full record

ArticleBMC cancer2022

Identification of TLN1 as a prognostic biomarker to effect cell proliferation and differentiation in acute myeloid leukemia.

Di Cui, Xilong Cui, Xiaoliang Xu, Wenjing Zhang, Yu Yu, Yingxin Gao, Chuanzhong Mei, Weiwei Zheng

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  7. Targeting Talin1 to reprogram dendritic cell activation landscapes: A mechanistically grounded cell therapy for multiple sclerosis model.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Article
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  9. Identification ofGenetics research · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Di Cui *Medical College, Fuyang Normal University, Fuyang, 236037, Anhui, China.
Xilong Cui *Spinal Deformity Clinical Medichine and Research Center of Anhui Province, 501 Sanqing Road, Fuyang, 236000, Anhui, China.
Xiaoliang Xu *School of Laboratory Medicine, Bengbu Medical College, Bengbu, 233030, Anhui, China.
Wenjing ZhangDivision of Life Sciences and Medicine, Department of Clinical Laboratory, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, 230001, Anhui, China.
Yu YuSchool of Laboratory Medicine, Bengbu Medical College, Bengbu, 233030, Anhui, China.
Yingxin GaoSchool of Laboratory Medicine, Bengbu Medical College, Bengbu, 233030, Anhui, China.
Chuanzhong MeiSchool of Laboratory Medicine, Bengbu Medical College, Bengbu, 233030, Anhui, China. meichzh@sina.com.
Weiwei ZhengDivision of Life Sciences and Medicine, Department of Clinical Laboratory, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, 230001, Anhui, China. zhengweiwei2009@163.com.
Bengbu Medical College · CNUniversity of Science and Technology of China · CNFuyang Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The protein Talin1 encoded by the TLN1 gene is a focal adhesion-related protein that binds to various cytoskeletal proteins and plays an important role in cell adhesion and movement. Recent studies have shown that it is overexpressed in prostate cancer, liver cancer, and oral squamous cell carcinoma, and is closely related to tumor progression and metastasis. This study integrated bioinformatics and functional analysis to reveal the prognosis and potential functions of TLN1 in AML. The results showed that the expression level of TLN1 was abnormally increased in AML and localized in the cell membrane and cytoplasm, and TLN1 is a significant prognostic indicator of overall survival (OS). Enrichment analysis of related genes showed that TLN1 is related to neutrophil mediated immunity, neutrophil activation and may regulate important signal pathways in hematological tumors including tyrosine kinase receptor, FLT3 and PIK3/AKT. The PPI network shows that TLN1 and MYH9 may be involved in the process of AML tumors together with PIP5K1C, ROCK1, S100A4, MY01A and WAC. Immune infiltration analysis explains that TLN1 is associated with multiple immune cells and may be an important immune marker in AML. Furthermore, molecular biology experiments confirmed that TLN1 is related to the proliferation, differentiation and cycle of AML cells. Silencing TLN1 can inhibit the proliferation of AML cells and promote differentiation through the Talin1/P-AKT/CREB signaling pathway.

Indexed as

Carcinoma, Squamous CellLeukemia, Myeloid, AcuteMouth NeoplasmsCell ProliferationCytoskeletal ProteinsHumansMalePrognosisProto-Oncogene Proteins c-aktReceptor Protein-Tyrosine Kinasesrho-Associated KinasesTalinCytoskeletal ProteinsProto-Oncogene Proteins c-aktReceptor Protein-Tyrosine Kinasesrho-Associated KinasesROCK1 protein, humanTalinTLN1 protein, humanAcute myeloid leukemiaMYH9PrognosticTalin1TLN1

Identifiers

PMID36175877
PMCPMC9520853
OpenAlexW4298001416

What OpenQuestion holds

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LicenceCC BY
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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.