Evidence map›Paper›PMID 38388484›Full record

ArticleCell death & disease2024

LAPTM4B-mediated hepatocellular carcinoma stem cell proliferation and MDSC migration: implications for HCC progression and sensitivity to PD-L1 monoclonal antibody therapy.

Haojun Wang, Quanwei Zhou, Ding Fang Xie, Qingguo Xu, Tongwang Yang, Wei Wang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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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

6 authors at 5 institutions in 1 country.

Haojun Wang *Department of Urology, Beijing Chaoyang Hospital, Capital Medical University, 100020, Beijing, China.ORCID 0000-0002-6604-9523
Quanwei Zhou *The National Key Clinical Specialty, Department of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Ding Fang XieThe Second Department of Medical Oncology, Xiangtan Central Hospital, Xiangtan, China.
Qingguo XuDepartment of Organ Transplant Center, The Affiliated Hospital of Qingdao University, Qingdao, China.
Tongwang YangThe Hunan Provincial University Key Laboratory of the Fundamentaland Clinical Research on Functional Nucleic Acid, Changsha Medical University, Changsha, China. 1203620677@qq.com.ORCID 0000-0002-6030-8416
Wei WangDepartment of Urology, Beijing Chaoyang Hospital, Capital Medical University, 100020, Beijing, China. weiwang0920@163.com.ORCID 0000-0003-2642-3338
Capital Medical University · CNChangsha Medical University · CNQingdao University · CNXiangyang Central Hospital · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In hepatocellular carcinoma (HCC), immunotherapy is vital for advanced-stage patients. However, diverse individual responses and tumor heterogeneity have resulted in heterogenous treatment outcomes. Our mechanistic investigations identified LAPTM4B as a crucial gene regulated by ETV1 (a transcription factor), especially in liver cancer stem cells (LCSCs). The influence of LAPTM4B on LCSCs is mediated via the Wnt1/c-Myc/β-catenin pathway. CXCL8 secretion by LAPTM4B drove myeloid-derived suppressor cell (MDSC) migration, inducing unfavorable patient prognosis. LAPTM4B affected PD-L1 receptor expression in tumor microenvironment and enhanced tumor suppression induced by PD-L1 monoclonal antibodies in HCC patients. LAPTM4B up-regulation is correlated with adverse outcomes in HCC patients, sensitizing them to PD-L1 monoclonal antibody therapy.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMyeloid-Derived Suppressor CellsAntibodies, MonoclonalB7-H1 AntigenCell ProliferationHumansImmunotherapyMembrane ProteinsOncogene ProteinsTranscription FactorsTumor MicroenvironmentAntibodies, MonoclonalB7-H1 AntigenLAPTM4B protein, humanMembrane ProteinsOncogene ProteinsTranscription Factors

Identifiers

PMID38388484
PMCPMC10884007
OpenAlexW4392058400

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.