Evidence map›Paper›PMID 33833983›Full record

ReviewFrontiers in oncology2021

PPAR-α Modulators as Current and Potential Cancer Treatments.

Yan Tan, Mina Wang, Ke Yang, Tiange Chi, Zehuan Liao, Peng Wei

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
9.0field-weighted citation impact, top 1% 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

68 citing papers in PubMed, 143 citations in OpenAlex.

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8 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

Yan TanSchool of Traditional Chinese Medicine and School of Life Sciences, Beijing University of Chinese Medicine, Beijing, China.
Mina WangSchool of Traditional Chinese Medicine and School of Life Sciences, Beijing University of Chinese Medicine, Beijing, China.
Ke YangSchool of Traditional Chinese Medicine and School of Life Sciences, Beijing University of Chinese Medicine, Beijing, China.
Tiange ChiThe First Clinical Medical School, Beijing University of Chinese Medicine, Beijing, China.
Zehuan LiaoSchool of Biological Sciences, Nanyang Technological University, Singapore, Singapore.
Peng WeiSchool of Traditional Chinese Medicine and School of Life Sciences, Beijing University of Chinese Medicine, Beijing, China.
Beijing University of Chinese Medicine · CNBeijing Hospital of Traditional Chinese Medicine · CNNanyang Technological University · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is one of the leading causes of mortality worldwide. PPAR modulators may hold great potential for the management of cancer patients. Indeed, PPARs are critical sensors and regulators of lipid, and they are able to promote eNOS activation, regulate immunity and inflammation response, and affect proliferation and differentiation of cancer cells. Cancer, a name given to a group of diseases, is characterized by multiple distinctive biological behaviors, including angiogenesis, abnormal cell proliferation, aerobic glycolysis, inflammation, etc. In the last decade, emerging evidence has shown that PPAR-α, a nuclear hormone receptor, can modulate carcinogenesis via exerting effects on one or several characteristic pathological behaviors of cancer. Therefore, the multi-functional PPAR modulators have substantial promise in various types of cancer therapies. This review aims to consolidate the functions of PPAR-α, as well as discuss the current and potential applications of PPAR-α agonists and antagonists in tackling cancer.

Indexed as

cancercancer treatmentPPAR-αPPAR-α agonistsPPAR-α antagonistsPPAR-α modulators

Identifiers

PMID33833983
PMCPMC8021859
OpenAlexW3136539940

What OpenQuestion holds

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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.