Evidence map›Paper›PMID 38517478›Full record

ArticleCancer reports (Hoboken, N.J.)2024

Long non-coding RNAFOXD1-AS1 modulated CTCs epithelial-mesenchymal transition and immune escape in hepatocellular carcinoma in vitro by sponging miR-615-3p.

Bao-Ling Guo, Qiu-Xiang Zheng, Yun-Shan Jiang, Ying Zhan, Wen-Jin Huang, Zhi-Yong Chen

Open access · goldAbstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Competing endogenous RNAs (ceRNAs) and drug resistance to cancer therapy.Cancer drug resistance (Alhambra, Calif.) · 2024
    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

6 authors at 1 institution in 1 country.

Bao-Ling GuoDepartment of Oncology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, People's Republic of China.
Qiu-Xiang ZhengDepartment of Oncology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, People's Republic of China.
Yun-Shan JiangDepartment of Oncology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, People's Republic of China.
Ying ZhanDepartment of Oncology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, People's Republic of China.
Wen-Jin HuangDepartment of Oncology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, People's Republic of China.
Zhi-Yong ChenDepartment of Oncology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, People's Republic of China.ORCID 0009-0005-0975-2449
Fujian Medical University · CN

Funding

Longyan City Science and Technology Plan Project 2020LYF17043
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is widely recognized as a globally prevalent malignancy. Immunotherapy is a promising therapy for HCC patients. Increasing evidence suggests that lncRNAs are involved in HCC progression and immunotherapy.

aimThe study reveals the mechanistic role of long non-coding RNA (lncRNA) FOXD1-AS1 in regulating migration, invasion, circulating tumor cells (CTCs), epithelial-mesenchymal transition (EMT), and immune escape in HCC in vitro.

methodsThis study employed real-time PCR (RT-qPCR) to measure FOXD1-AS1, miR-615-3p, and programmed death-ligand 1 (PD-L1). The interactions of FOXD1-AS1, miR-615-3p, and PD-L1 were validated via dual-luciferase reporter gene and ribonucleoprotein immunoprecipitation (RIP) assay. In vivo experimentation involves BALB/c mice and BALB/c nude mice to investigate the impact of HCC metastasis.

resultsThe upregulation of lncRNA FOXD1-AS1 in malignant tissues significantly correlates with poor prognosis. The investigation was implemented on the impact of lncRNA FOXD1-AS1 on the migratory, invasive, and EMT of HCC cells. It has been observed that the lncRNA FOXD1-AS1 significantly influences the generation and metastasis of

conclusionThis study presents compelling evidence supporting the role of lncRNA FOXD1-AS1 as a miRNA sponge that sequesters miR-655-3p and protects PD-L1 from suppression.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicroRNAsRNA, Long NoncodingAnimalsB7-H1 AntigenCell Line, TumorEpithelial-Mesenchymal TransitionForkhead Transcription FactorsHumansMiceMice, NudePhosphatidylinositol 3-KinasesB7-H1 AntigenForkhead Transcription FactorsFOXD1 protein, humanMicroRNAsMIRN615 microRNA, humanMIRN655 microRNA, humanPhosphatidylinositol 3-KinasesRNA, Long NoncodingCTChepatocellular carcinomaimmune escapelncRNA FOXD1‐AS1PD‐L1

Identifiers

PMID38517478
PMCPMC10959247
OpenAlexW4393098346

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.