Evidence map›Paper›PMID 36463330›Full record

ArticleCommunications biology2022

Surveying lncRNA-lncRNA cooperations reveals dominant effect on tumor immunity cross cancers.

Tingting Shao, Yunjin Xie, Jingyi Shi, Changbo Yang, Haozhe Zou, Yongsheng Li, Juan Xu, Xia Li

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. LncRNATranslational cancer research · 2024
    Article
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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

8 authors at 2 institutions in 1 country.

Tingting Shao *College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China.
Yunjin Xie *College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China.
Jingyi Shi *College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China.
Changbo YangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China.
Haozhe ZouCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China.
Yongsheng LiKey Laboratory of Tropical Translational Medicine of Ministry of Education, College of Biomedical Information and Engineering, Hainan Women and Children's Medical Center, Hainan Medical University, Haikou, 571199, China. liyongsheng@ems.hrbmu.edu.cn.
Juan XuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China. xujuanbiocc@ems.hrbmu.edu.cn.ORCID 0000-0002-3709-4165
Xia LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China. lixia@hrbmu.edu.cn.ORCID 0000-0002-9794-2648
Harbin Medical University · CNHainan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long non-coding RNAs (lncRNAs) can crosstalk with each other by post-transcriptionally co-regulating genes involved in the same or similar functions; however, the regulatory principles and biological insights in tumor-immune are still unclear. Here, we show a multiple-step model to identify lncRNA-lncRNA immune cooperation based on co-regulating functional modules by integrating multi-omics data across 20 cancer types. Moreover, lncRNA immune cooperative networks (LICNs) are constructed, which are likely to modulate tumor-immune microenvironment by regulating immune-related functions. We highlight conserved and rewired network hubs which can regulate interactions between immune cells and tumor cells by targeting ligands and activating or inhibitory receptors such as PDCD1, CTLA4 and CD86. Immune cooperative lncRNAs (IC-lncRNAs) playing central roles in many cancers also tend to target known anticancer drug targets. In addition, these IC-lncRNAs tend to be highly expressed in immune cell populations and are significantly correlated with immune cell infiltration. The similar immune mechanisms cross cancers are revealed by the LICNs. Finally, we identify two subtypes of skin cutaneous melanoma with different immune context and prognosis based on IC-lncRNAs. In summary, this study contributes to a comprehensive understanding of the cooperative behaviours of lncRNAs and accelerating discovery of lncRNA-based biomarkers in cancer.

Indexed as

MelanomaRNA, Long NoncodingSkin NeoplasmsCutaneous Malignant MelanomaHumansTumor MicroenvironmentRNA, Long Noncoding

Identifiers

PMID36463330
PMCPMC9719535
OpenAlexW4310779119

What OpenQuestion holds

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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.