Evidence map›Paper›PMID 29636841›Full record

ReviewOxidative medicine and cellular longevity2018

Regulation of Tumor Progression by Programmed Necrosis.

Su Yeon Lee, Min Kyung Ju, Hyun Min Jeon, Eui Kyong Jeong, Yig Ji Lee, Cho Hee Kim, Hye Gyeong Park, Song Iy Han, Ho Sung Kang

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed, 3 pooled it
6.8field-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

124 citing papers in PubMed, 3 syntheses or guidelines pooled it, 209 citations in OpenAlex.

  1. Changes in Tissue Fluidity Predict Tumor Aggressiveness In Vivo.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Pooled it
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  9. Two-color spheroid model for determining the OJournal of biological engineering · 2026
    Article
  10. Ubiquitin-conjugating Enzymes in Cancer.International journal of biological sciences · 2026
    Review
  11. Metabolic Gadolinium Labeling ofBiomaterials research · 2026
    Article
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64 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

9 authors at 3 institutions in 1 country.

Su Yeon LeeDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan 609-735, Republic of Korea.ORCID 0000-0002-9401-2306
Min Kyung JuDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan 609-735, Republic of Korea.ORCID 0000-0001-9574-7294
Hyun Min JeonDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan 609-735, Republic of Korea.
Eui Kyong JeongDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan 609-735, Republic of Korea.
Yig Ji LeeDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan 609-735, Republic of Korea.
Cho Hee KimDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan 609-735, Republic of Korea.
Hye Gyeong ParkNanobiotechnology Center, Pusan National University, Pusan 609-735, Republic of Korea.
Song Iy HanThe Division of Natural Medical Sciences, College of Health Science, Chosun University, Gwangju 501-759, Republic of Korea.ORCID 0000-0003-4975-480X
Ho Sung KangDepartment of Molecular Biology, College of Natural Sciences, Pusan National University, Pusan 609-735, Republic of Korea.ORCID 0000-0002-8449-9907
Pusan National University · KRChosun University · KRNational Forensic Institute · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rapidly growing malignant tumors frequently encounter hypoxia and nutrient (e.g., glucose) deprivation, which occurs because of insufficient blood supply. This results in necrotic cell death in the core region of solid tumors. Necrotic cells release their cellular cytoplasmic contents into the extracellular space, such as high mobility group box 1 (HMGB1), which is a nonhistone nuclear protein, but acts as a proinflammatory and tumor-promoting cytokine when released by necrotic cells. These released molecules recruit immune and inflammatory cells, which exert tumor-promoting activity by inducing angiogenesis, proliferation, and invasion. Development of a necrotic core in cancer patients is also associated with poor prognosis. Conventionally, necrosis has been thought of as an unregulated process, unlike programmed cell death processes like apoptosis and autophagy. Recently, necrosis has been recognized as a programmed cell death, encompassing processes such as oncosis, necroptosis, and others. Metabolic stress-induced necrosis and its regulatory mechanisms have been poorly investigated until recently. Snail and Dlx-2, EMT-inducing transcription factors, are responsible for metabolic stress-induced necrosis in tumors. Snail and Dlx-2 contribute to tumor progression by promoting necrosis and inducing EMT and oncogenic metabolism. Oncogenic metabolism has been shown to play a role(s) in initiating necrosis. Here, we discuss the molecular mechanisms underlying metabolic stress-induced programmed necrosis that promote tumor progression and aggressiveness.

Indexed as

ApoptosisAutophagyCell DeathDisease ProgressionHumansNecrosisNeoplasms

Identifiers

PMID29636841
PMCPMC5831895
OpenAlexW2785327608

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.