Evidence map›Paper›PMID 39279925›Full record

ArticleJournal of gastrointestinal oncology2024

NOVA2 regulates the properties of liver cancer stem cells and lenvatinib resistance in hepatocellular carcinoma via the Wnt pathway.

Jing-Zhu Cao, Chao-Qun Wang, Zheng Shi, Jing-Yun Song, Francisco Tustumi, Tiago Biachi de Castria, Jennifer Wu, Christine Pocha, Diamantis I Tsilimigras, Zhi-Hong Wang and 2 more

Abstract read
In one paragraph

Article in Journal of gastrointestinal oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. 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

12 authors.

Jing-Zhu Cao *Department of Endocrinology, Changhai Hospital, Naval Medical University, Shanghai, China.
Chao-Qun Wang *Department of Endocrinology, Changhai Hospital, Naval Medical University, Shanghai, China.
Zheng Shi *Department of Gastrointestinal Surgery, Changhai Hospital, Naval Medical University, Shanghai, China.
Jing-Yun SongDepartment of Endocrinology, Changhai Hospital, Naval Medical University, Shanghai, China.
Francisco TustumiDepartment of Gastroenterology, Digestive Surgery Division, University of São Paulo Medical School, Sao Paulo, Brazil.
Tiago Biachi de CastriaMoffitt Cancer Center, Tampa, FL, USA.
Jennifer WuDivision of Hematology and Oncology, Perlmutter Cancer Center of NYU Langone Health, NYU Grossman School of Medicine, New York, NY, USA.
Christine PochaSanford School of Medicine, University of South Dakota, Avera Hepatology and Transplant, Sioux Falls, SD, USA.
Diamantis I TsilimigrasDivision of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center and James Comprehensive Cancer Center, Columbus, OH, USA.
Zhi-Hong WangThe Third Department of Hepatic Surgery, Eastern Hepatobiliary Surgery Hospital, Naval Medical University, Shanghai, China.
Tao TaoDepartment of Endocrinology and Metabolism, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Jin LuDepartment of Endocrinology, Changhai Hospital, Naval Medical University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The regulation of cancer stem cells (CSCs) is influenced by RNA-binding proteins (RBPs). The present study sought to investigate the role of NOVA2 in the processes of self-renewal, carcinogenesis, and lenvatinib resistance in liver CSCs. Methods: Neuro-oncological ventral antigen 2 (NOVA2) expression in liver CSCs was examined by real-time polymerase chain reaction (PCR). Results: In our study, the expression of the RBP NOVA2 was higher in CSCs. NOVA2 also increased the capacity for self-renewal and carcinogenesis of the liver CSCs via the Wnt pathway. Further, suppressing the Wnt pathway leads to desensitization of the hepatocellular carcinoma (HCC) cells that overexpress NOVA2 to apoptosis caused by lenvatinib. Analyzing patient data confirmed reduced levels of NOVA2 and therefore we speculate that NOVA2 may serve as a potential indicator for response to lenvatinib in patients with HCC. Methyltransferase-like 3 (METTL3) and YTH N6-methyladenosine RNA-binding protein 1 (YTHDF1)-dependent N6-methyladenosine (m Conclusions: NOVA2 is involved in the process of liver CSC self-renewal and carcinogenesis. In addition, NOVA2 expression may help identify patients with a higher chance of benefiting from lenvatinib treatment and can be a promising therapeutic target for HCC.

Indexed as

hepatocellular carcinoma (HCC)lenvatinibLiver cancer stem cell (liver CSC)N6-methyladenosine (m6A)neuro-oncological ventral antigen 2 (NOVA2)

Identifiers

PMID39279925
PMCPMC11399850

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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.