Evidence map›Paper›PMID 31257364›Full record

ArticleCancer gene therapy2020

Targeting mTOR suppressed colon cancer growth through 4EBP1/eIF4E/PUMA pathway.

Huanan Wang, Yeying Liu, Jie Ding, Yuan Huang, Jing Liu, Nannan Liu, Yue Ao, Yi Hong, Lefeng Wang, Lingling Zhang and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  5. PI3K/Akt/mTOR Signaling Pathway as a Target for Colorectal Cancer Treatment.International journal of molecular sciences · 2024
    Review
  6. Article
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  9. Liquid Biopsy by ctDNA in Liver Transplantation for Colorectal Cancer Liver Metastasis.Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract · 2023
    Article
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  11. Review
  12. Review
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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

12 authors at 4 institutions in 1 country.

Huanan Wang *Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Yeying Liu *College of Biology, Hunan University, Changsha, China.
Jie Ding *Department of Emergency Surgery, The Second Military Medical University, Shanghai, China.
Yuan HuangCollege of Biology, Hunan University, Changsha, China.
Jing LiuCollege of Biology, Hunan University, Changsha, China.
Nannan LiuCollege of Biology, Hunan University, Changsha, China.
Yue AoDepartment of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Yi HongDepartment of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Lefeng WangDepartment of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou, China.
Lingling ZhangDepartment of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, China.
Jiangang WangDepartment of Health Management, The Third Xiangya Hospital, Central South University, Changsha, China. wangzigangcsu@hotmail.com.
Yingjie ZhangCollege of Biology, Hunan University, Changsha, China. yingjiezhang@hnu.edu.cn.ORCID http://orcid.org/0000-0002-9207-2364
Hunan University · CNCentral South University · CNZhejiang University · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer is the third most frequently diagnosed malignancies among both men and women, which has an increased mortality but a poor prognosis. Targeting mTOR becomes an effective approach that shows promising antitumor activities in various cancers including colonic carcinoma. However, the potential mechanism against colon cancer remains incompletely understood. Here, we demonstrated that the anti-cancer effect of AZD8055 and OSI-027 is at least in part modulated by the gradual process of apoptosis initiation, progressing from mTOR suppression, 4EBP1 dephosphorylation, or EZH2 suppression, thereby leading to PUMA-dependent apoptosis via the intrinsic mitochondrial pathway. Furthermore, AZD8055 inhibited colorectal cancer tumor growth in mice significantly. PUMA deletion caused resistance of dual mTOR inhibitors, suggesting PUMA mediated carcinogenesis in vitro and in vivo. Collectively, these findings established a vital status of PUMA in driving the antineoplastic efficacy of targeting mTOR by AZD8055 and OSI-027 and offered the rationales for the current clinical assessment.

Indexed as

AnimalsApoptosis Regulatory ProteinsColonic NeoplasmsDNA-Binding ProteinsFemaleHCT116 CellsHumansImidazolesMiceMice, Inbred BALB CMice, NudeMolecular Targeted TherapyMorpholinesProto-Oncogene ProteinsSignal TransductionSirolimus(5-(2,4-bis((3S)-3-methylmorpholin-4-yl)pyrido(2,3-d)pyrimidin-7-yl)-2-methoxyphenyl)methanolApoptosis Regulatory ProteinsBBC3 protein, humanDNA-Binding ProteinsELF4 protein, humanImidazolesMorpholinesMTOR protein, humanOSI 027Proto-Oncogene ProteinsSirolimusTOR Serine-Threonine KinasesTranscription FactorsTriazines

Identifiers

PMID31257364
OpenAlexW2954884543

What OpenQuestion holds

Textmetadata
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.