Evidence map›Paper›PMID 40655469›Full record

ArticleJournal of hepatocellular carcinoma2025

Hsa_circ_0007991 Promotes Immune Evasion in Hepatocellular Carcinoma via Regulation of the miR-505-3p/CANX Axis.

LingLing Wang, Li Liang, Jing Qian, Chao Yu, Yu Shi, XiaoDi Yan, Xiang Chen

Abstract read
In one paragraph

Article in Journal of hepatocellular carcinoma, 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. 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

7 authors.

LingLing Wang *Department of Clinical Laboratory, Nantong First People's Hospital, Nantong City, Jiangsu Province, 226000, People's Republic of China.
Li Liang *Department of Interventional, Nantong First People's Hospital, Nantong City, Jiangsu Province, 226000, People's Republic of China.
Jing QianDepartment of Tumor Radiotherapy, Affiliated Hospital of Nantong University, Nantong City, Jiangsu Province, 226001, People's Republic of China.
Chao YuDepartment of Clinical Laboratory, Nantong First People's Hospital, Nantong City, Jiangsu Province, 226000, People's Republic of China.
Yu ShiDepartment of Tumor Radiotherapy, Affiliated Hospital of Nantong University, Nantong City, Jiangsu Province, 226001, People's Republic of China.
XiaoDi YanDepartment of Tumor Radiotherapy, Affiliated Hospital of Nantong University, Nantong City, Jiangsu Province, 226001, People's Republic of China.
Xiang ChenDepartment of Clinical Laboratory, Nantong First People's Hospital, Nantong City, Jiangsu Province, 226000, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aimed to investigate the expression and functional role of hsa_circ_0007991 in hepatocellular carcinoma (HCC). Methods: RNA expression data of HCC and corresponding non-tumor liver tissues were obtained from the GEO database, and differential expression analysis was conducted to identify significantly dysregulated circRNAs. A total of 68 clinical samples from HCC patients were collected, and hsa_circ_0007991 level was quantified using RT-qPCR. Gain- and loss-of-function experiments were performed on HCC cells, followed by assessments of cellular proliferation, apoptosis, and immune evasion using CCK-8, EdU incorporation assays, flow cytometry, and ELISA. The role of hsa_circ_0007991 as a ceRNA was further validated using dual-luciferase reporter assay, RNA immunoprecipitation, and nuclear-cytoplasmic fractionation. Results: A significant upregulation of hsa_circ_0007991 was observed in HCC tissues, with increased levels correlating with advanced TNM stages. hsa_circ_0007991 silencing significantly suppressed HCC cell proliferation and immune evasion, while promoting apoptosis, whereas hsa_circ_0007991 overexpression yielded the opposite effects. The function of hsa_circ_0007991 involves binding to miR-505-3p, which modulates the expression of calnexin (CANX), influencing the biological behaviors of HCC cells. Rescue experiments validated the essential function of the hsa_circ_0007991/miR-505-3p/CANX pathway in HCC. Conclusion: hsa_circ_0007991 is upregulated in HCC and closely associated with tumor proliferation and immune evasion by regulating the miR-505-3p/CANX axis.

Indexed as

hepatocellular carcinomahsa_circ_0007991immune evasionproliferation

Identifiers

PMID40655469
PMCPMC12254195

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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.