Evidence map›Paper›PMID 36429010›Full record

ArticleCells2022

Targeting Wnt/β-Catenin Signaling Exacerbates Ferroptosis and Increases the Efficacy of Melanoma Immunotherapy via the Regulation of MITF.

Hao Wang, Hengxiang Zhang, Yuhan Chen, Huina Wang, Yangzi Tian, Xiuli Yi, Qiong Shi, Tao Zhao, Baolu Zhang, Tianwen Gao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 51 citations in OpenAlex.

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  19. Ferroptosis: CD8Cell death discovery · 2025
    Review
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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

13 authors at 2 institutions in 1 country.

Hao WangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Hengxiang ZhangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Yuhan ChenDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Huina WangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Yangzi TianDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Xiuli YiDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Qiong ShiDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Tao ZhaoDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Baolu ZhangDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Tianwen GaoDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Sen GuoDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Chunying LiDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Weinan GuoDepartment of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is the most lethal form of skin cancer, resulting from the malignant transformation of epidermal melanocytes. Recent revolutionary progress in targeted therapy and immunotherapy has prominently improved the treatment outcome, but the survival of melanoma patients remains suboptimal. Ferroptosis is greatly involved in cancer pathogenesis and can execute the outcome of immunotherapy. However, the detailed regulatory mechanisms of melanoma cell ferroptosis remain elusive. Herein, we report that Wnt/β-catenin signaling regulates ferroptosis and melanoma immunotherapy efficacy via the regulation of MITF. First of all, we found that Wnt/β-catenin signaling was prominently suppressed in melanoma cell ferroptosis. Then, we proved that targeting β-catenin exacerbated melanoma cell ferroptosis by promoting the generation of lipid peroxidation both in vitro and in vivo. Subsequent mechanistic studies revealed that MITF mediated the effect of Wnt/β-catenin signaling on melanoma cell ferroptosis, and PGC1α and SCD1 were documented as two main effectors downstream of Wnt/β-catenin-MITF pathway. Ultimately, pharmacological inhibition of β-catenin or MITF increased the efficacy of anti-PD-1 immunotherapy in preclinical xenograft tumor model by promoting ferroptosis. Taken together, Wnt/β-catenin signaling deficiency exacerbates ferroptosis in melanoma via the regulation of MITF. Targeting Wnt/β-catenin-MITF pathway could be a promising strategy to potentiate ferroptosis and increase the efficacy of anti-PD-1 immunotherapy.

Indexed as

FerroptosisMelanomabeta CateninHumansImmunotherapyMicrophthalmia-Associated Transcription FactorWnt ProteinsWnt Signaling Pathwaybeta CateninMicrophthalmia-Associated Transcription FactorMITF protein, humanWnt Proteinsanti-PD-1 immunotherapyferroptosismelanomaMITFWnt/β-catenin

Identifiers

PMID36429010
PMCPMC9688625
OpenAlexW4309003743

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.