Evidence map›Paper›PMID 35116073›Full record

ArticleComputational and mathematical methods in medicine2022

G-Protein-Coupled Receptor Kinase-Interacting Protein 1 (GIT1) Promotes Head and Neck Squamous Cell Carcinoma Metastases via Activating the PI3K/AKT/mTOR Signal Pathway.

Runze Xu, Ran Xu, Yuanxiang Wang, Weixing Wang, Lingling Jiang, Shishun Gong

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Computational and mathematical methods in medicine, 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 It has been retracted, and should not be counted.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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. [Study on the correlation between high expression of GIT1 and M2 macrophage infiltration and prognosis in hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Article
  2. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Runze XuGraduate School, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China.
Ran XuCentre of Cancer Diagnosis and Treatment, JiangSu Rudong County People's Hospital, Nantong 226400, China.
Yuanxiang WangDepartment of Obstetrics and Gynecology, JiangSu Rudong Country People's Hospital, Nantong 226400, China.
Weixing WangCentre of Cancer Diagnosis and Treatment, JiangSu Rudong County People's Hospital, Nantong 226400, China.
Lingling JiangDepartment of Medical Nursing, JiangSu Rudong Country People's Hospital, Nantong 226400, China.
Shishun GongDepartment of Rehabilitation, Hainan Medical College, Haikou, 571199 Hainan, China.ORCID https://orcid.org/0000-0001-6912-021X
Shanghai Jiao Tong University · CNHainan Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGIT1 is identified as a novel tumor oncogene in breast cancer. In this article, we aimed to explore the role of GIT1 in the progression of head and neck squamous cell carcinoma (HNSCC).

methodsGIT1 expression in HNSCC was detected by RT-qPCR, immunohistochemistry assay, and Western blot. HNSCC cell proliferation, migration, and invasion were examined by CCK-8 assay, Wound healing assay, and Transwell assay, respectively. Cell apoptosis was detected by flow cytometric analysis.

resultsIn our study, GIT1 was notably upregulated in HNSCC tissues and cells. Moreover, GIT1 expression level had positive corelation with pathological grade and nodal status of HNSCC. Functional experiments showed that knockdown of GIT1 restrained HNSCC proliferation, invasion, migration, and EMT and facilitated cell apoptosis. Furthermore, GIT1 knockdown was found to restrain HNSCC tumor growth and lung metastasis. Additionally, PI3K/AKT/mTOR signal pathway inhibitors suppressed the effect of GIT1 on HNSCC cell progression.

conclusionGIT1 was upregulated in HNSCC and facilitated HNSCC cell progression by inducing PI3K/AKT/mTOR signal pathway. Therefore, we suggested that GIT1 might be a potential target for HNSCC treatment.

Indexed as

Adaptor Proteins, Signal TransducingAgedAnimalsApoptosisCell Cycle ProteinsCell Line, TumorCell MovementCell ProliferationComputational BiologyFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHead and Neck NeoplasmsHeterograftsHumansMaleAdaptor Proteins, Signal TransducingCell Cycle ProteinsGIT1 protein, humanMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID35116073
PMCPMC8807036
OpenAlexW4210419513

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.