Evidence map›Paper›PMID 34200642›Full record

ArticleGenes2021

LncRNA FENDRR Expression Correlates with Tumor Immunogenicity.

Maria Cristina Munteanu, Sri Nandhini Sethuraman, Mohit Pratap Singh, Jerry Malayer, Ashish Ranjan

Abstract read
In one paragraph

Article in Genes, 2021. 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
–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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. The role of LncRNAs in tumor immunotherapy.Cancer cell international · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Long Noncoding RNAInternational journal of molecular sciences · 2021
    Article
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

5 authors.

Maria Cristina MunteanuCollege of Veterinary Medicine, Physiological Sciences, Oklahoma State University, Stillwater, OK 74074, USA.
Sri Nandhini SethuramanCollege of Veterinary Medicine, Physiological Sciences, Oklahoma State University, Stillwater, OK 74074, USA.
Mohit Pratap SinghCollege of Veterinary Medicine, Physiological Sciences, Oklahoma State University, Stillwater, OK 74074, USA.
Jerry MalayerCollege of Veterinary Medicine, Physiological Sciences, Oklahoma State University, Stillwater, OK 74074, USA.ORCID 0000-0002-6955-8374
Ashish RanjanCollege of Veterinary Medicine, Physiological Sciences, Oklahoma State University, Stillwater, OK 74074, USA.ORCID 0000-0001-8851-496X

Funding

Novel focused ultrasound enhanced calreticulin-nanoparticle for immune primed melanoma immunotherapyR37CA239150 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI RANJAN, ASHISH · 2019 to 2025
$2.9M
NCI NIH HHS R37 CA239150
6 · The paper itself

Abstract

FENDRR (Fetal-lethal non-coding developmental regulatory RNA, LncRNA FOXF1-AS1) is a recently identified tumor suppressor long non-coding (LncRNA) RNA, and its expression has been linked with epigenetic modulation of the target genes involved in tumor immunity. In this study, we aimed to understand the role of FENDRR in predicting immune-responsiveness and the inflammatory tumor environment. Briefly, FENDRR expression and its relationship to immune activation signals were assessed in murine cell lines. Data suggested that tumor cells (e.g., C26 colon, 4T1 breast) that typically upregulate immune activation genes and the MHC class I molecule exhibited high FENDRR expression levels. Conversely, tumor cells with a generalized downregulation of immune-related gene expression (e.g., B16F10 melanoma) demonstrated low to undetectable FENDRR levels. Mechanistically, the modulation of FENDRR expression enhanced the inflammatory and WNT signaling pathways in tumors. Our early data suggest that FENDRR can play an important role in the development of immune-relevant phenotypes in tumors, and thereby improve cancer immunotherapy.

Indexed as

AnimalsBiomarkers, TumorCell Line, TumorColonic NeoplasmsHistocompatibility Antigens Class IHumansMelanomaMiceMice, Inbred C57BLRNA, Long NoncodingWnt Signaling PathwayBiomarkers, TumorHistocompatibility Antigens Class IRNA, Long NoncodingbiomarkerFENDRRimmunotherapytumor immunogenicity

Identifiers

PMID34200642
PMCPMC8226633

What Socratic 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 Socratic graph.