Evidence map›Paper›PMID 37283803›Full record

ArticleJournal of Cancer2023

CC-115 Mediates GSDME-Dependent Pyroptosis in Lung Adenocarcinoma Through the Akt/Bax Pathway.

Ting Zhang, Ming-Quan Liu, Guang-Su Xie, Dong-Ming Wu, Peng-Wei Luo, Teng Liu, Shi-Hua Deng, Yuan-Yi Wang, Shuang He, Ye Zhou and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 25% 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, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Diagnostic and prognostic value of the gasdermins in gastric cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
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 1 institution in 1 country.

Ting ZhangSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Ming-Quan LiuSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Guang-Su XieXindu District People's Hospital of Chengdu, Chengdu 610500, China.
Dong-Ming WuSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Peng-Wei LuoSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Teng LiuSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Shi-Hua DengSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Yuan-Yi WangSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Shuang HeSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Ye ZhouSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
Jin ZhouSichuan Cancer Hospital and Institute, School of Medicine, University of Electronic Science and Technology, Sichuan 610042, China.
Ying XuSchool of Clinical Medicine & The First Affiliated Hospital of Chengdu Medical College, Chengdu 610500, China.
First Affiliated Hospital of Chengdu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapeutic agents remain the first-line treatment for solid tumors, including lung cancer, but chemotherapy resistance is hampering global efforts to treat this disease. CC-115 is a novel antitumoral compound used in phase I clinical trials. However, it is unclear whether CC-115 is effective against lung adenocarcinoma (LUAD). In the present study, we found that CC-115 induced lytic cell death in A549 and H1650 tumor cells via swelling of cells and formation of large bubbles on the plasma membrane that closely resembled those typical of pyroptosis, a type of programmed cell death linked to chemotherapy. We demonstrated that CC-115 exerts antitumor effects in LUAD through gasdermin E (GSDME)-mediated pyroptosis by acting as a dual inhibitor of DNA-PK and mTOR. CC-115 can inhibit Akt phosphorylation, impairing its inhibitory effect on Bax, thereby inducing pyroptosis via the Bax-mitochondrial intrinsic pathway. CC-115-induced pyroptosis was abrogated by treatment with the Akt activator SC79 or by depletion of Bax. Importantly, CC-115 significantly upregulated the expression of Bax and GSDME-N in a xenograft mouse model, with a reduction in tumor size. Our results revealed that CC-115 suppresses tumor growth by inducing GSDME-mediated pyroptosis through the Akt/Bax-mitochondrial intrinsic pathway, indicating CC-115 as a promising therapeutic agent for LUAD.

Indexed as

BaxCC-115chemotherapyGSDMElung adenocarcinomapyroptosis

Identifiers

PMID37283803
PMCPMC10240660
OpenAlexW4379599943

What OpenQuestion holds

Textmetadata
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.