Evidence map›Paper›PMID 39414994›Full record

ArticleCommunications biology2024

RABIF promotes hepatocellular carcinoma progression through regulation of mitophagy and glycolysis.

Ning Feng, Rui Zhang, Xin Wen, Wei Wang, Nie Zhang, Junnian Zheng, Longzhen Zhang, Nianli Liu

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. bioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. 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

8 authors.

Ning Feng *Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Rui Zhang *Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xin WenCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Wei WangCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Nie ZhangCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Junnian ZhengCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Longzhen ZhangDepartment of Radiation Oncology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China. jsxyfyzlz1@163.com.ORCID 0009-0009-4220-4224
Nianli LiuCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China. liunli@xzhmu.edu.cn.ORCID 0000-0002-0602-6709

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81972165National Natural Science Foundation of China (National Science Foundation of China) 81972845
6 · The paper itself

Abstract

The RAB interacting factor (RABIF) is a putative guanine nucleotide exchange factor that also functions as a RAB-stabilizing holdase chaperone. It has been implicated in pathogenesis of several cancers. However, the functional role and molecular mechanism of RABIF in hepatocellular carcinoma (HCC) are not entirely known. Here, we demonstrate an upregulation of RABIF in patients with HCC, correlating with a poor prognosis. RABIF inhibition results in decreased HCC cell growth both in vitro and in vivo. Our study reveals that depleting RABIF attenuates the STOML2-PARL-PGAM5 axis-mediated mitophagy. Consequently, this reduction in mitophagy results in diminished mitochondrial reactive oxygen species (mitoROS) production, thereby alleviating the HIF1α-mediated downregulation of glycolytic genes HK1, HKDC1, and LDHB. Additionally, we illustrate that RABIF regulates glucose uptake by controlling RAB10 expression. Importantly, the knockout of RABIF or blockade of mitophagy sensitizes HCC cells to sorafenib. This study uncovers a previously unrecognized role of RABIF crucial for HCC growth and identifies it as a potential therapeutic target.

Indexed as

Carcinoma, HepatocellularGlycolysisLiver NeoplasmsMitophagyAnimalsCell Line, TumorDisease ProgressionGene Expression Regulation, NeoplasticGuanine Nucleotide Exchange FactorsHumansMaleMembrane ProteinsMiceMice, Nuderab GTP-Binding ProteinsGuanine Nucleotide Exchange FactorsMembrane ProteinsRab10 protein, humanrab GTP-Binding ProteinsRABIF protein, human

Identifiers

PMID39414994
PMCPMC11484875

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.