Evidence map›Paper›PMID 34926131›Full record

ArticleAnalytical cellular pathology (Amsterdam)2021

Anlotinib Suppresses Oral Squamous Cell Carcinoma Growth and Metastasis by Targeting the RAS Protein to Inhibit the PI3K/Akt Signalling Pathway.

Yunfei Lu, Jing Lin, Meng Duan, Ying Rui, Hao Zheng, Liting Zhu, Xuanyu Zhu, Jingchen Wei

Open access · goldAbstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 13 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

8 authors at 2 institutions in 1 country.

Yunfei LuCollege of Pharmacy, Guilin Medical University, Guilin 541199, China.ORCID https://orcid.org/0000-0001-5363-6836
Jing LinDepartment of Medical Oncology, The Affiliated Hospital of Guilin Medical University, Guilin 541001, China.
Meng DuanResearch Lab of Translational Medicine, Heng Yang Medical University, University of South China, Hengyang 421001, China.ORCID https://orcid.org/0000-0002-5679-2946
Ying RuiCollege of Pharmacy, Guilin Medical University, Guilin 541199, China.
Hao ZhengCollege of Pharmacy, Guilin Medical University, Guilin 541199, China.ORCID https://orcid.org/0000-0003-1969-8499
Liting ZhuCollege of Pharmacy, Guilin Medical University, Guilin 541199, China.ORCID https://orcid.org/0000-0002-1459-1599
Xuanyu ZhuCollege of Pharmacy, Guilin Medical University, Guilin 541199, China.
Jingchen WeiCollege of Pharmacy, Guilin Medical University, Guilin 541199, China.ORCID https://orcid.org/0000-0002-5117-8832
Guilin Medical University · CNUniversity of South China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral squamous cell carcinoma (OSCC) is a malignant tumour originating from the mucosal lining of the oral cavity. Its characteristics include hidden onset, high recurrence, and distant metastasis after operation. At present, clinical treatment usually includes surgery, chemotherapy, radiotherapy, or the joint use of these modalities. Unfortunately, multidrug resistant is one of the important obstacles that causes cancer chemotherapy failure. Anlotinib, which has recently been proven to have good antitumour effects, is a novel multitargeted tyrosine kinase inhibitor. However, there are few studies of the anlotinib-associated mechanism in OSCC and its underlying molecular mechanism. In our study, in vitro models of human oral squamous cell carcinoma HSC-3 cells were used to determine the efficacy of anlotinib. On the one hand, we showed that anlotinib treatment significantly reduced the viability and proliferation of HSC-3 cells and decreased cell migration by inhibiting the activation of the Akt phosphorylation pathway. On the other side, anlotinib inhibited PI3K/Akt/Bad phosphorylation and promoted apoptosis of HSC-3 cells by activating RAS protein expression. In brief, these results indicated that anlotinib had prominent antitumour activity in OSCC, mainly by inhibiting the PI3K/Akt phosphorylation pathway. This work provides evidences and a basic principle for using anlotinib to treat patients with OSCC for clinical research.

Indexed as

ApoptosisBlotting, WesternCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationDose-Response Relationship, DrugHumansIndolesMouth NeoplasmsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktQuinolinesras ProteinsSignal TransductionanlotinibIndolesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktQuinolinesras Proteins

Identifiers

PMID34926131
PMCPMC8674064
OpenAlexW4200175810

What OpenQuestion holds

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LicenceCC BY
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.