Evidence map›Paper›PMID 36012397›Full record

ArticleInternational journal of molecular sciences2022

Metformin Mitigated Obesity-Driven Cancer Aggressiveness in Tumor-Bearing Mice.

Chun-Jung Chen, Chih-Cheng Wu, Cheng-Yi Chang, Jian-Ri Li, Yen-Chuan Ou, Wen-Ying Chen, Su-Lan Liao, Jiaan-Der Wang

Open access · goldFull text read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 17 citations in OpenAlex.

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  5. HMGB1: A Central Node in Cancer Therapy Resistance.International journal of molecular sciences · 2025
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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 6 institutions in 1 country.

Chun-Jung ChenDepartment of Medical Research, Taichung Veterans General Hospital, Taichung City 407, Taiwan.
Chih-Cheng WuDepartment of Anesthesiology, Taichung Veterans General Hospital, Taichung City 407, Taiwan.
Cheng-Yi ChangDepartment of Surgery, Feng Yuan Hospital, Taichung City 420, Taiwan.
Jian-Ri LiDivision of Urology, Taichung Veterans General Hospital, Taichung City 407, Taiwan.
Yen-Chuan OuDivision of Urology, Tungs' Taichung Metro Harbor Hospital, Taichung City 435, Taiwan.
Wen-Ying ChenDepartment of Veterinary Medicine, National Chung Hsing University, Taichung City 402, Taiwan.ORCID 0000-0002-5105-5285
Su-Lan LiaoDepartment of Medical Research, Taichung Veterans General Hospital, Taichung City 407, Taiwan.
Jiaan-Der WangChildren's Medical Center, Taichung Veterans General Hospital, Taichung City 407, Taiwan.
National Chung Hsing University · TWTaichung Veterans General Hospital · TWChina Medical University · TWProvidence University · TWTunghai University · TWTungs' Taichung MetroHarbor Hospital · TW

Funding

Ministry of Science and Technology, Taiwan MOST 108-2314-B-075A-004Taichung Veterans General Hospital TCVGH-1057327D, 1096508C, 1106501C, 1116501C, YM1090102
6 · The paper itself

Abstract

Metformin may offer benefits to certain cancer populations experiencing metabolic abnormalities. To extend the anticancer studies of metformin, a tumor model was established through the implantation of murine Lewis Lung Carcinoma (LLC) cells to Normal Diet (ND)-fed and High-Fat Diet (HFD)-fed C57BL/6 mice. The HFD-fed mice displayed metabolic and pro-inflammatory alterations together with accompanying aggressive tumor growth. Metformin mitigated tumor growth in HFD-fed mice, paralleled by reductions in circulating glucose, insulin, soluble P-selectin, TGF-β1 and High Mobility Group Box-1 (HMGB1), as well as tumor expression of cell proliferation, aerobic glycolysis, glutaminolysis, platelets and neutrophils molecules. The suppressive effects of metformin on cell proliferation, migration and oncogenic signaling molecules were confirmed in cell study. Moreover, tumor-bearing HFD-fed mice had higher contents of circulating and tumor immunopositivity of Neutrophil Extracellular Traps (NETs)-associated molecules, with a suppressive effect from metformin. Data taken from neutrophil studies confirmed the inhibitory effect that metformin has on NET formation induced by HMGB1. Furthermore, HMGB1 was identified as a promoting molecule to boost the transition process towards NETs. The current study shows that metabolic, pro-inflammatory and NET alterations appear to play roles in the obesity-driven aggressiveness of cancer, while also representing candidate targets for anticancer potential of metformin.

Indexed as

HMGB1 ProteinMetforminNeoplasmsAnimalsDiet, High-FatMiceMice, Inbred C57BLObesityHMGB1 ProteinMetforminmetabolismmetforminneutrophil extracellular trapsneutrophilsobesitysalignancy

Identifiers

PMID36012397
PMCPMC9408975
OpenAlexW4292068946

What OpenQuestion holds

Textfull text, public
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.