Evidence map›Paper›PMID 39619229›Full record

ReviewMedComm2024

Programmed cell death: molecular mechanisms, biological functions, diseases, and therapeutic targets.

Shen'er Qian, Yao Long, Guolin Tan, Xiaoguang Li, Bo Xiang, Yongguang Tao, Zuozhong Xie, Xiaowei Zhang

Abstract readReview
In one paragraph

Review in MedComm, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

50 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. In vitro study and in silico reveal Teucrium Polium L. methanolic extract as an apoptosis inducer and a potential Bcl-2 inhibitor for breast cancer.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
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  6. A β‑1,3‑1,6‑glucan fromMolecular medicine reports · 2026
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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

8 authors.

Shen'er QianDepartment of Otolaryngology Head and Neck Surgery The Third Xiangya Hospital, Central South University Changsha Hunan China.
Yao LongCancer Research Institute School of Basic Medicine Central South University Changsha Hunan China.
Guolin TanDepartment of Otolaryngology Head and Neck Surgery The Third Xiangya Hospital, Central South University Changsha Hunan China.
Xiaoguang LiDepartment of Otolaryngology Head and Neck Surgery Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine Shanghai China.
Bo XiangCancer Research Institute School of Basic Medicine Central South University Changsha Hunan China.
Yongguang TaoCancer Research Institute School of Basic Medicine Central South University Changsha Hunan China.ORCID https://orcid.org/0000-0003-2354-5321
Zuozhong XieDepartment of Otolaryngology Head and Neck Surgery The Second Xiangya Hospital Central South University Changsha Hunan China.ORCID https://orcid.org/0000-0001-7114-4464
Xiaowei ZhangDepartment of Otolaryngology Head and Neck Surgery The Third Xiangya Hospital, Central South University Changsha Hunan China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed cell death represents a precisely regulated and active cellular demise, governed by a complex network of specific genes and proteins. The identification of multiple forms of programmed cell death has significantly advanced the understanding of its intricate mechanisms, as demonstrated in recent studies. A thorough grasp of these processes is essential across various biological disciplines and in the study of diseases. Nonetheless, despite notable progress, the exploration of the relationship between programmed cell death and disease, as well as its clinical application, are still in a nascent stage. Therefore, further exploration of programmed cell death and the development of corresponding therapeutic methods and strategies holds substantial potential. Our review provides a detailed examination of the primary mechanisms behind apoptosis, autophagy, necroptosis, pyroptosis, and ferroptosis. Following this, the discussion delves into biological functions and diseases associated dysregulated programmed cell death. Finally, we highlight existing and potential therapeutic targets and strategies focused on cancers and neurodegenerative diseases. This review aims to summarize the latest insights on programmed cell death from mechanisms to diseases and provides a more reliable approach for clinical transformation.

Indexed as

cancerscell homeostasisclinical transformationneurodegenerative disordersprogrammed cell death

Identifiers

PMID39619229
PMCPMC11604731

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.