Evidence map›Paper›PMID 36913368›Full record

ArticlePloS one2023

Chaperone-mediated autophagy promotes breast cancer angiogenesis via regulation of aerobic glycolysis.

Rui Chen, Peng Li, Yan Fu, Zongyao Wu, Lijun Xu, Junhua Wang, Sha Chen, Mingzhen Yang, Bingjie Peng, Yao Yang and 3 more

Open access · goldFull text read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.6field-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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Polygonatum sibiricum component liquiritigenin restrains breast cancer cell invasion and migration by inhibiting HSP90 and chaperone-mediated autophagy.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2024
    Article
  8. Review
  9. Article
  10. Review
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

13 authors at 4 institutions in 1 country.

Rui ChenTibetan Traditional Medical College, Lhasa, China.
Peng LiYantai Mountain Hospital, Yantai, Shandong, China.
Yan FuGeneral Hospital, Western Theater Command, Chengdu, Sichuan, China.
Zongyao WuTibetan Traditional Medical College, Lhasa, China.
Lijun XuTibetan Traditional Medical College, Lhasa, China.
Junhua WangGeneral Hospital of Tibet Area Military Command, Lhasa, China.
Sha ChenArmy Medical University (Third Military Medical University), Chongqing, China.
Mingzhen YangArmy Medical University (Third Military Medical University), Chongqing, China.
Bingjie PengArmy Medical University (Third Military Medical University), Chongqing, China.
Yao YangGeneral Hospital, Western Theater Command, Chengdu, Sichuan, China.
Hongwei ZhangGeneral Hospital of Tibet Area Military Command, Lhasa, China.
Qi HanGeneral Hospital of Tibet Area Military Command, Lhasa, China.
Shuhui LiArmy Medical University (Third Military Medical University), Chongqing, China.ORCID 0000-0002-1697-5334
Army Medical University · CNTibetan Traditional Medical College · CNTibet Autonomous Region People's Hospital · CNYantaishan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence shows that chaperone-mediated autophagy (CMA) is involved in cancer cell pathogenesis and progression. However, the potential role of CMA in breast cancer angiogenesis remains unknown. We first manipulated CMA activity by knockdown and overexpressing of lysosome-associated membrane protein type 2A (LAMP2A) in MDA-MB-231, MDA-MB-436, T47D and MCF7 cells. We found that the tube formation, migration and proliferation abilities of human umbilical vein endothelial cells (HUVECs) were inhibited after cocultured with tumor-conditioned medium from breast cancer cells of LAMP2A knockdown. While the above changes were promoted after cocultured with tumor-conditioned medium from breast cancer cells of LAMP2A overexpression. Moreover, we found that CMA could promote VEGFA expression in breast cancer cells and in xenograft model through upregulating lactate production. Finally, we found that lactate regulation in breast cancer cells is hexokinase 2 (HK2) dependent, and knockdown of HK2 can significantly reduce the ability of CMA-mediated tube formation capacity of HUVECs. Collectively, these results indicate that CMA could promote breast cancer angiogenesis via regulation of HK2-dependent aerobic glycolysis, which may serve as an attractive target for breast cancer therapies.

Indexed as

Breast NeoplasmsChaperone-Mediated AutophagyAutophagyCell Line, TumorCulture Media, ConditionedFemaleGlycolysisHumansHuman Umbilical Vein Endothelial CellsLysosomal-Associated Membrane Protein 2Lysosomal Membrane ProteinsCulture Media, ConditionedLysosomal-Associated Membrane Protein 2Lysosomal Membrane Proteins

Identifiers

PMID36913368
PMCPMC10010525
OpenAlexW4324019780

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read35
reference markers read2
identifiers read7
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.