Evidence map›Paper›PMID 32839434›Full record

ArticleCell death & disease2020

Transcriptome profiling analysis reveals that ATP6V0E2 is involved in the lysosomal activation by anlotinib.

Xin Sun, Yuhan Shu, Peiyi Yan, Hongliang Huang, Ruilan Gao, Mengting Xu, Liqin Lu, Jingkui Tian, Dongsheng Huang, Jianbin Zhang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 44 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

10 authors at 6 institutions in 1 country.

Xin Sun *Department of Oncology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.
Yuhan Shu *College of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, China.
Peiyi Yan *Department of Clinical Laboratory, Shanghai Putuo District People's Hospital, Shanghai, China.
Hongliang HuangSchool of Biosciences & Biopharmaceutics and Center for Bioresources & Drug Discovery, Guangdong Pharmaceutical University, Guangzhou, China.
Ruilan GaoInstitution of Hematology Research, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Mengting XuCollege of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, China.
Liqin LuDepartment of Oncology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.
Jingkui TianCollege of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, China. tjk@zju.edu.cn.
Dongsheng HuangKey Laboratory of Tumor Molecular Diagnosis and Individualized Medicine of Zhejiang Province, Clinical Research Institute, People's Hospital of Hangzhou Medical College, Hangzhou, China. dshuang@zju.edu.cn.
Jianbin ZhangDepartment of Oncology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China. zhangjianbin@hmc.edu.cn.
Zhejiang University · CNHangzhou Medical College · CNZhejiang Provincial People's Hospital · CNCentral Hospital of Putuo District · CNGuangdong Pharmaceutical University · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anlotinib is a receptor tyrosine kinase inhibitor with potential anti-neoplastic and anti-angiogenic activities. It has been approved for the treatment of non-small-cell lung cancer. Lysosomes are acidic organelles and have been implicated in various mechanisms of cancer therapeutics. However, the effect of anlotinib on lysosomal function has not been investigated. In the present study, anlotinib induces apoptosis in human colon cancer cells. Through transcriptome sequencing, we found for the first time that anlotinib treatment upregulates ATP6V0E2 (ATPase H

Indexed as

AnimalsApoptosisAutophagosomesAutophagyBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarcinoma, Non-Small-Cell LungCell Line, TumorCell NucleusColonic NeoplasmsGene Expression ProfilingHumansIndolesLung NeoplasmsLysosomesMaleMechanistic Target of Rapamycin Complex 1anlotinibBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsIndolesMechanistic Target of Rapamycin Complex 1MTOR protein, humanQuinolinesReceptor Protein-Tyrosine KinasesTOR Serine-Threonine Kinases

Identifiers

PMID32839434
PMCPMC7445181
OpenAlexW3080657314

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.