Evidence map›Paper›PMID 37346933›Full record

ArticleMedComm2023

Sanggenon C inhibits cell proliferation and induces apoptosis by regulating the MIB1/DAPK1 axis in glioblastoma.

Hongbo Chang, Jianbing Hou, Yaqian Shao, Minghao Xu, Xuelian Weng, Yi Du, Junbo Shi, Li Zhang, Hongjuan Cui

Open access · goldAbstract read
In one paragraph

Article in MedComm, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 15 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

9 authors at 3 institutions in 2 countries.

Hongbo ChangState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Jianbing HouState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Yaqian ShaoState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Minghao XuState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Xuelian WengState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Yi DuState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Junbo ShiState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Li ZhangDepartment of Radiology and Nuclear Medicine The First Hospital of HeBei Medical University Hebei China.
Hongjuan CuiState Key Laboratory of Resource Insects Medical Research Institute Southwest University Chongqing China.
Southwest University · CNFirst Affiliated Hospital of Hebei Medical University · CNZero to Three · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sanggenon C (SC), a herbal flavonoid extracted from Cortex Mori, has been mentioned to possess more than one treasured organic properties. However, the molecular mechanism of its anti-tumor impact in glioblastoma (GBM) remains unclear. In this study, we reported that SC displayed a GBM-suppressing impact in vitro and in vivo with no apparent organ toxicity. SC dramatically suppressed cell proliferation-induced cell apoptosis in GBM cells. Mechanistically, we unveiled that SC modulated the protein expression of death associated protain kinase 1 (DAPK1) by controlling the ubiquitination and degradation of DAPK1. Quantitative proteomic and Western blot analyses showed that SC improved DAPK1 protein degradation via decreasing the expression of E3 ubiquitin ligase Mindbomb 1 (MIB1). More importantly, the effects of SC on cell proliferation and apoptosis of GBM cells have been in part reversed through DAPK1 downregulation or MIB1 overexpression, respectively. These results indicated that SC might suppress cell proliferation and induce cell apoptosis by decreasing MIB1-mediated DAPK1 degradation. Furthermore, we found that SC acted synergistically with temozolomide (TMZ), an anti-cancer drug used in GBM, resulting in elevated chemotherapeutic sensitivity of GBM to TMZ. Collectively, our data suggest that SC might be a promising anti-cancer agent for GBM therapy.

Indexed as

chemosensitivityDAPK1glioblastomaMIB1sanggenon C

Identifiers

PMID37346933
PMCPMC10279945
OpenAlexW4381432200

What Socratic 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 Socratic graph.