Evidence map›Paper›PMID 35725836›Full record

ReviewSignal transduction and targeted therapy2022

Autophagy, ferroptosis, pyroptosis, and necroptosis in tumor immunotherapy.

Weitong Gao, Xueying Wang, Yang Zhou, Xueqian Wang, Yan Yu

Open access · goldAbstract readReview
In one paragraph

Review in Signal transduction and targeted therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 624 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
624citing papers in PubMed, 2 pooled it
141.2field-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

624 citing papers in PubMed, 2 syntheses or guidelines pooled it, 959 citations in OpenAlex.

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  12. Disulfidptosis: molecular mechanisms and therapeutic targets.Signal transduction and targeted therapy · 2026
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564 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

5 authors at 2 institutions in 1 country.

Weitong Gao *Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Xueying Wang *Department of Otolaryngology Head and Neck Surgery, Xiangya Hospital, Central South University, changsha, 410008, China.
Yang ZhouDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Xueqian WangDepartment of Head and Neck Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Yan YuDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, China. gpyuyan@126.com.
Third Affiliated Hospital of Harbin Medical University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, immunotherapy represented by immune checkpoint inhibitors (ICIs) has led to unprecedented breakthroughs in cancer treatment. However, the fact that many tumors respond poorly or even not to ICIs, partly caused by the absence of tumor-infiltrating lymphocytes (TILs), significantly limits the application of ICIs. Converting these immune "cold" tumors into "hot" tumors that may respond to ICIs is an unsolved question in cancer immunotherapy. Since it is a general characteristic of cancers to resist apoptosis, induction of non-apoptotic regulated cell death (RCD) is emerging as a new cancer treatment strategy. Recently, several studies have revealed the interaction between non-apoptotic RCD and antitumor immunity. Specifically, autophagy, ferroptosis, pyroptosis, and necroptosis exhibit synergistic antitumor immune responses while possibly exerting inhibitory effects on antitumor immune responses. Thus, targeted therapies (inducers or inhibitors) against autophagy, ferroptosis, pyroptosis, and necroptosis in combination with immunotherapy may exert potent antitumor activity, even in tumors resistant to ICIs. This review summarizes the multilevel relationship between antitumor immunity and non-apoptotic RCD, including autophagy, ferroptosis, pyroptosis, and necroptosis, and the potential targeting application of non-apoptotic RCD to improve the efficacy of immunotherapy in malignancy.

Indexed as

FerroptosisNeoplasmsAutophagyHumansImmunologic FactorsImmunotherapyNecroptosisPyroptosisImmunologic Factors

Identifiers

PMID35725836
PMCPMC9208265
OpenAlexW4283156085

What OpenQuestion holds

Textmetadata
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.