Evidence map›Paper›PMID 31467365›Full record

ArticleCancer gene therapy2020

Alkaliptosis: a new weapon for cancer therapy.

Jiao Liu, Feimei Kuang, Rui Kang, Daolin Tang

Open access · bronzeAbstract readEditorial
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

76 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Metabolic cell death in cancer: mechanisms and therapeutic potential.Apoptosis : an international journal on programmed cell death · 2025
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Programmed cell death in lung cancer: mechanisms, immune responses, and therapeutics.Apoptosis : an international journal on programmed cell death · 2026
    Review
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16 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

4 authors at 4 institutions in 2 countries.

Jiao LiuThe Third Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Feimei KuangThe Third Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China.
Rui KangDepartment of Surgery, UT Southwestern Medical Center, Dallas, TX, USA.
Daolin TangThe Third Affiliated Hospital, Guangzhou Medical University, Guangzhou, Guangdong, China. daolin.tang@utsouthwestern.edu.
Guangzhou Medical University · CNSouthwestern Medical Center · USThe University of Texas Southwestern Medical Center · USThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant tumors are one of the major causes of death worldwide, and the development of better treatments is urgently needed. There are many types of cancer treatment, such as surgery, chemotherapy, radiation therapy, immunotherapy, and targeted therapy, that might improve patient outcomes in a genotype- and stage-dependent manner. The main goal of cancer therapy is to inhibit biological capabilities of tumors and eventually eliminate the cancer cells. However, cancer cells are well known to escape apoptosis, a form of programmed cell death that was first described in studies of cell development and tissue remodelling. Increasing our understanding of cell death may result in new anticancer approaches that target types of nonapoptotic cell death, such as necroptosis, ferroptosis, autophagy-dependent cell death, and alkaliptosis. Notably, alkaliptosis, a pH-dependent form of regulated cell death, has been recently identified as a new strategy for cancer therapy across multiple tumor types, especially in pancreatic cancer.

Indexed as

AminoquinolinesAntigens, NeoplasmAntineoplastic AgentsBenzamidesCarbonic Anhydrase IXCell Line, TumorCell SurvivalDown-RegulationDrug DevelopmentHumansHydrogen-Ion ConcentrationNF-kappa BPancreatic NeoplasmsRegulated Cell DeathSignal TransductionAminoquinolinesAntigens, NeoplasmAntineoplastic AgentsBenzamidesCA9 protein, humanCarbonic Anhydrase IXN-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamideNF-kappa B

Identifiers

PMID31467365
OpenAlexW2971004704

What OpenQuestion holds

Textmetadata
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.