Evidence map›Paper›PMID 30332964›Full record

ReviewCurrent cancer drug targets2019

The Multifunctional Protein p62 and Its Mechanistic Roles in Cancers.

Shunbin Ning, Ling Wang

Open access · greenAbstract readReview
In one paragraph

Review in Current cancer drug targets, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

27 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. The Roles of SQSTM1/p62 in Selective Autophagy and Oncogenic Signaling.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. p66shc deficiency attenuates high glucose-induced autophagy dysfunction in Schwann cells.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Article
  12. The Autophagy ReceptorViruses · 2024
    Article
  13. Article
  14. Denosumab Induces Neoplastic Stromal Cell ApoptosisCurrent cancer drug targets · 2024
    Article
  15. Article
  16. Article
  17. Cells · 2023
    Article
  18. Article
  19. Article
  20. Review
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

2 authors at 1 institution in 1 country.

Shunbin NingDivision of Infectious Diseases, Department of Internal Medicine, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
Ling WangDivision of Infectious Diseases, Department of Internal Medicine, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, United States.
East Tennessee State University · US

Funding

Targeting the Oncogenic Transcription Factor IRF4 in Hematological MalignanciesR15DE029621 · NIDCR · EAST TENNESSEE STATE UNIVERSITY · PI NING, SHUNBIN · 2021 to 2021
$447k
LIMD1 Is a Novel Marker Associated with IRF4 in EBV Latency and LymphomaR15DE027314 · NIDCR · EAST TENNESSEE STATE UNIVERSITY · PI NING, SHUNBIN · 2017 to 2017
$444k
NIDCR NIH HHS R15 DE027314NIDCR NIH HHS R15 DE029621
6 · The paper itself

Abstract

The multifunctional signaling hub p62 is well recognized as a ubiquitin sensor and a selective autophagy receptor. As a ubiquitin sensor, p62 promotes NFκB activation by facilitating TRAF6 ubiquitination and aggregation. As a selective autophagy receptor, p62 sorts ubiquitinated substrates including p62 itself for lysosome-mediated degradation. p62 plays crucial roles in myriad cellular processes including DNA damage response, aging/senescence, infection and immunity, chronic inflammation, and cancerogenesis, dependent on or independent of autophagy. Targeting p62-mediated autophagy may represent a promising strategy for clinical interventions of different cancers. In this review, we summarize the transcriptional and post-translational regulation of p62, and its mechanistic roles in cancers, with the emphasis on its roles in regulation of DNA damage response and its connection to the cGAS-STING-mediated antitumor immune response, which is promising for cancer vaccine design.

Indexed as

AutophagyCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseHumansMembrane ProteinsNeoplasmsNucleotidyltransferasesProteolysisRNA-Binding ProteinsSignal TransductionSTING ProteinUbiquitinationcGAS protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseMembrane ProteinsNucleotidyltransferasesP62 protein, humanRNA-Binding ProteinsSTING1 protein, humanSTING Proteinantitumor immune responseautophagycancer vaccine designp62ROSubiquitination.

Identifiers

PMID30332964
PMCPMC8052633
OpenAlexW2897849579

What OpenQuestion holds

Textmetadata
LicenceTDM
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.