Evidence map›Paper›PMID 40189704›Full record

ArticleOncogene2025

Dichotomous roles of ACBD3 in NSCLC growth and metastasis.

Xiaochao Tan, Chao Wu, Priyam Banerjee, Shike Wang, Derrick L Cardin, Yuting Xu, Chad J Creighton, William K Russell

Abstract read
In one paragraph

Article in Oncogene, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Xiaochao TanDepartment of Medicine, Tulane University School of Medicine, Louisiana Cancer Research Center, New Orleans, LA, USA. xtan4@tulane.edu.ORCID http://orcid.org/0000-0002-8603-5700
Chao WuDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas-MD Anderson Cancer Center, Houston, TX, USA.
Priyam BanerjeeDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas-MD Anderson Cancer Center, Houston, TX, USA.
Shike WangDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas-MD Anderson Cancer Center, Houston, TX, USA.
Derrick L CardinDepartment of Medicine, Tulane University School of Medicine, Louisiana Cancer Research Center, New Orleans, LA, USA.
Yuting XuDepartment of Medicine, Tulane University School of Medicine, Louisiana Cancer Research Center, New Orleans, LA, USA.
Chad J CreightonDepartment of Medicine and Dan L Duncan Cancer Center, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0002-6090-703X
William K RussellDepartment of Biochemistry and Molecular Biology, The University of Texas Medical Branch, Galveston, TX, USA.

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Suzanne AW Fuqua · 2007 to 2026
$73.9M
An actionable secretory program that drives tumor progression in a genetically defined subset of lung squamous carcinomaR03CA280382 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI TAN, XIAOCHAO · 2023 to 2024
$158k
NCI NIH HHS P30 CA125123NCI NIH HHS R03 CA280382U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) NIH CA125123
6 · The paper itself

Abstract

Lung cancer continues to be the leading cause of cancer-related deaths globally. Unraveling the regulators behind lung cancer growth and its metastatic spread, along with understanding the underlying mechanisms, is crucial for developing novel and effective therapeutic strategies. While much research has focused on identifying potential oncogenes or tumor suppressors, the roles of certain genes can vary depending on the context and may even exhibit contradictory effects. In this study, we demonstrate that acyl-CoA binding domain containing 3 (ACBD3), a Golgi resident protein, promotes primary lung cancer growth by recruiting phosphatidylinositol (PI)-4-kinase IIIβ (PI4KB) to the Golgi, thereby enhancing oncogenic secretion in chromosome 1q-amplified lung cancer cells. Conversely, in chromosome 1q-diploid lung cancer cells, ACBD3 acts as a suppressor of lung cancer metastasis by inhibiting the NOTCH signaling pathway and reducing cancer cell motility. This highlights the intricacy of cancer progression and cautions against simplistic approaches targeting individual oncogenes for cancer therapy.

Indexed as

Adaptor Proteins, Signal TransducingCarcinoma, Non-Small-Cell LungLung NeoplasmsMembrane ProteinsAnimalsCell Line, TumorCell MovementCell ProliferationGolgi ApparatusHumansMiceNeoplasm MetastasisReceptors, NotchSignal TransductionAdaptor Proteins, Signal TransducingMembrane ProteinsReceptors, Notch

Identifiers

PMID40189704
PMCPMC12167707

What Socratic 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 Socratic graph.