Evidence map›Paper›PMID 38447939›Full record

ArticleAutophagy2024

CLU (clusterin) and PPARGC1A/PGC1α coordinately control mitophagy and mitochondrial biogenesis for oral cancer cell survival.

Prakash P Praharaj, Srimanta Patra, Amruta Singh, Debasna P Panigrahi, Hwa Y Lee, Mohammad F Kabir, Muhammad K Hossain, Samir K Patra, Birija S Patro, Shankargouda Patil and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Autophagy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  4. HSP90α lactylation orchestrates PGC1α and LRPGC1 nuclear translocation driving mitochondrial biogenesis.Proceedings of the National Academy of Sciences of the United States of America · 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

13 authors at 6 institutions in 3 countries.

Prakash P PraharajCancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology Rourkela, Rourkela, Odisha, India.ORCID 0000-0003-0425-5118
Srimanta PatraCancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology Rourkela, Rourkela, Odisha, India.ORCID 0000-0002-0166-0903
Amruta SinghCancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology Rourkela, Rourkela, Odisha, India.ORCID 0000-0002-8551-7708
Debasna P PanigrahiCancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology Rourkela, Rourkela, Odisha, India.ORCID 0000-0001-6707-8062
Hwa Y LeeDepartment of Pharmacology, Jeonbuk National University Medical School, Jeonju, Jeonbuk, Republic of Korea.ORCID 0000-0001-9365-5863
Mohammad F KabirDepartment of Pharmacology, School of Medicine, Institute of New Drug Development, Jeonbuk National University, Jeonju, Republic of Korea.ORCID 0000-0001-5019-6062
Muhammad K HossainSchool of Pharmacy, Jeonbuk National University, Jeonju, Jeonbuk, Republic of Korea.ORCID 0000-0003-2132-2984
Samir K PatraLaboratory of epigenetics, Department of Life Science, National Institute of Technology Rourkela, Rourkela, Odisha, India.ORCID 0000-0001-5641-1835
Birija S PatroBio-Organic Division, Bhabha Atomic Research Centre, Mumbai, Maharashtra, India.ORCID 0000-0001-9161-5913
Shankargouda PatilCollege of Dental Medicine, Roseman University of Health Sciences, South Jordan, UT, USA.ORCID 0000-0001-7246-5497
Daniel J KlionskyLife Sciences Institute and Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-7828-8118
Han J ChaeSchool of Pharmacy, Jeonbuk National University, Jeonju, Jeonbuk, Republic of Korea.ORCID 0000-0003-4190-9889
Sujit K BhutiaCancer and Cell Death Laboratory, Department of Life Science, National Institute of Technology Rourkela, Rourkela, Odisha, India.ORCID 0000-0003-0962-3354
National Institute of Technology Rourkela · INJeonbuk National University · KRBhabha Atomic Research Centre · INJeonbuk National University Hospital · KRRoseman University of Health Sciences · USUniversity of Michigan · US

Funding

ALTERNATIVE VACUOLAR TARGETING MECHANISMS IN YEASTR01GM053396 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KLIONSKY, DANIEL J. · 1995 to 2018
$12.1M
The mechanism and regulation of autophagyR35GM131919 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DANIEL J. KLIONSKY · 2019 to 2026
$6.4M
NIGMS NIH HHS R01 GM053396NIGMS NIH HHS R35 GM131919
6 · The paper itself

Abstract

Mitophagy involves the selective elimination of defective mitochondria during chemotherapeutic stress to maintain mitochondrial homeostasis and sustain cancer growth. Here, we showed that CLU (clusterin) is localized to mitochondria to induce mitophagy controlling mitochondrial damage in oral cancer cells. Moreover, overexpression and knockdown of CLU establish its mitophagy-specific role, where CLU acts as an adaptor protein that coordinately interacts with BAX and LC3 recruiting autophagic machinery around damaged mitochondria in response to cisplatin treatment. Interestingly, CLU triggers class III phosphatidylinositol 3-kinase (PtdIns3K) activity around damaged mitochondria, and inhibition of mitophagic flux causes the accumulation of excessive mitophagosomes resulting in reactive oxygen species (ROS)-dependent apoptosis during cisplatin treatment in oral cancer cells. In parallel, we determined that PPARGC1A/PGC1α (PPARG coactivator 1 alpha) activates mitochondrial biogenesis during CLU-induced mitophagy to maintain the mitochondrial pool. Intriguingly, PPARGC1A inhibition through small interfering RNA (si

Indexed as

Cell SurvivalClusterinMitochondriaMitophagyMouth NeoplasmsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaAnimalsApoptosisAutophagyCell Line, TumorCisplatinHumansMiceMice, NudeOrganelle BiogenesisReactive Oxygen SpeciesCisplatinCLU protein, humanClusterinPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanReactive Oxygen SpeciesClusterinmitochondrial biogenesismitophagymitophagy-associated cell deathPPARGC1A/PGC1α

Identifiers

PMID38447939
PMCPMC11210931
OpenAlexW4392757382

What OpenQuestion holds

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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.