Evidence map›Paper›PMID 33082557›Full record

ArticleOncogene2021

Metabolic reprogramming of ovarian cancer involves ACSL1-mediated metastasis stimulation through upregulated protein myristoylation.

Qingyu Zhang, Wei Zhou, Shan Yu, Yaojun Ju, Sally Kit Yan To, Alice Sze Tsai Wong, Yufei Jiao, Terence Chuen Wai Poon, Kin Yip Tam, Leo Tsz On Lee

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 57 citations in OpenAlex.

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  14. Ferroptosis is an effective strategy for cancer therapy.Medical oncology (Northwood, London, England) · 2024
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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

10 authors at 5 institutions in 3 countries.

Qingyu Zhang *Cancer Centre, Faculty of Health Sciences, University of Macau, Taipa, Macau, China.
Wei Zhou *State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 210009, Nanjing, China.
Shan YuCancer Centre, Faculty of Health Sciences, University of Macau, Taipa, Macau, China.
Yaojun JuProteomics, Metabolomics and Drug Development Core, Faculty of Health Sciences, University of Macau, Taipa, Macau, China.
Sally Kit Yan ToSchool of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
Alice Sze Tsai WongSchool of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong, China.
Yufei JiaoDepartment of Pathology, The Second Affiliated Hospital of Harbin Medical University, 150001, Harbin, China.
Terence Chuen Wai PoonProteomics, Metabolomics and Drug Development Core, Faculty of Health Sciences, University of Macau, Taipa, Macau, China.
Kin Yip TamProteomics, Metabolomics and Drug Development Core, Faculty of Health Sciences, University of Macau, Taipa, Macau, China.
Leo Tsz On LeeCancer Centre, Faculty of Health Sciences, University of Macau, Taipa, Macau, China. LTOLee@um.edu.mo.
University of Macau · MOUniversity of Hong Kong · HKAffiliated Hospital of Guangdong Medical College Hospital · CNChina Pharmaceutical University · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As a result of the hostile microenvironment, metabolic alterations are required to enable the malignant growth of cancer cells. To understand metabolic reprogramming during metastasis, we conducted shotgun proteomic analysis of highly metastatic (HM) and non-metastatic (NM) ovarian cancer cells. The results suggest that the genes involved in fatty-acid (FA) metabolism are upregulated, with consequent increases of phospholipids with relatively short FA chains (myristic acid, MA) in HM cells. Among the upregulated proteins, ACSL1 expression could convert the lipid profile of NM cells to that similar of HM cells and make them highly aggressive. Importantly, we demonstrated that ACSL1 activates the AMP-activated protein kinase and Src pathways via protein myristoylation and finally enhances FA beta oxidation. Patient samples and tissue microarray data also suggested that omentum metastatic tumours have higher ACSL1 expression than primary tumours and a strong association with poor clinical outcome. Overall, our data reveal that ACSL1 enhances cancer metastasis by regulating FA metabolism and myristoylation.

Indexed as

Up-RegulationAnimalsCarcinoma, Ovarian EpithelialCell Line, TumorCoenzyme A LigasesFatty AcidsFemaleGene Expression Regulation, NeoplasticHumansLipidomicsMiceNeoplasm MetastasisNeoplasm TransplantationOvarian NeoplasmsPrognosisProteomicsACSL1 protein, humanCoenzyme A LigasesFatty Acids

Identifiers

PMID33082557
OpenAlexW3094077964

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.