Evidence map›Paper›PMID 36567598›Full record

ReviewTechnology in cancer research & treatment

Biological Role and Mechanism of Lipid Metabolism Reprogramming Related Gene ECHS1 in Cancer.

Teng Hu, Xiaojing Chen, Simin Lu, Hao Zeng, Lu Guo, Yunwei Han

Open access · goldAbstract readReview
In one paragraph

Review in Technology in cancer research & treatment. 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
1.7field-weighted citation impact, top 14% 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, 21 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

6 authors at 1 institution in 1 country.

Teng HuDepartment of Oncology, 556508The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Xiaojing ChenDepartment of Oncology, 556508The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Simin LuDepartment of Oncology, 556508The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Hao ZengDepartment of Oncology, 556508The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Lu GuoDepartment of Ophthalmology, 556508The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Yunwei HanDepartment of Oncology, 556508The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.ORCID 0000-0001-8330-0444
Affiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a major threat to human health today. Although the existing anticancer treatments have effectively improved the prognosis of some patients, there are still other patients who cannot benefit from these well-established strategies. Reprogramming of lipid metabolism is one of the typical features of cancers. Recent studies have revealed that key enzymes involved in lipid metabolism may be effective anticancer therapeutic targets, but the development of therapeutic lipid metabolism targets is still insufficient. ECHS1 (enoyl-CoA hydratase, short chain 1) is a key enzyme mediating the hydration process of mitochondrial fatty acid β-oxidation and has been observed to be abnormally expressed in a variety of cancers. Therefore, with ECHS1 and cancer as the main keywords, we searched the relevant studies of ECHS1 in the field of cancer in Pubmed, summarized the research status and functions of ECHS1 in different cancer contexts, and explored its potential regulatory mechanisms, with a view to finding new therapeutic targets for anti-metabolic therapy. By reviewing and summarizing the retrieved literatures, we found that ECHS1 regulates malignant biological behaviors such as cell proliferation, metastasis, apoptosis, autophagy, and drug resistance by remodeling lipid metabolism and regulating intercellular oncogenic signaling pathways. Not only that, ECHS1 exhibits early diagnostic and prognostic value in clear cell renal cell carcinoma, and small-molecule inhibitors that regulate ECHS1 also show therapeutic significance in preclinical studies. Taken together, we propose that ECHS1 has the potential to serve as a therapeutic target of lipid metabolism.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsCell ProliferationHumansLipid MetabolismSignal Transductionbiomarkercancerenoyl-CoA hydratase, short chain 1fatty acids β-oxidationlipid metabolism reprogramming

Identifiers

PMID36567598
PMCPMC9806408
OpenAlexW4313019304

What OpenQuestion holds

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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.