Evidence map›Paper›PMID 34406628›Full record

ArticleHuman cell2021

Highly expressed TLX1NB and NPSR1-AS1 lncRNAs could serve as diagnostic tools in colorectal cancer.

Shaghayegh Dastjerdi, Mehdi Valizadeh, Rasoul Nemati, Mohammad Amin Honardoost, Nasrin Fattahi Dolatabadi, Atefeh Zamani, Hossein Tabatabaeian

Abstract read
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Article in Human cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. Article
  5. Article
  6. MIMT1 and LINC01550 are uncharted lncRNAs down-regulated in colorectal cancer.International journal of experimental pathology · 2023
    Article
  7. Article
  8. Article
  9. 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 at 4 institutions in 1 country.

Shaghayegh Dastjerdi *Gene Raz Bu Ali, Genetic and Biotechnology Academy, Isfahan, Iran.
Mehdi Valizadeh *Unit of Genomics Research, Digestive Diseases Research Center, Ardabil University of Medical Sciences, Ardabil, Iran.
Rasoul NematiDepartment of Internal Medicine, School of Medicine and Allied Medical Sciences, Digestive Diseases Research Center, Ardabil University of Medical Sciences, Ardabil, Iran.
Mohammad Amin HonardoostDepartment of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.
Nasrin Fattahi DolatabadiGene Raz Bu Ali, Genetic and Biotechnology Academy, Isfahan, Iran.
Atefeh ZamaniGene Raz Bu Ali, Genetic and Biotechnology Academy, Isfahan, Iran.
Hossein TabatabaeianDepartment of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran. csiht@nus.edu.sg.ORCID http://orcid.org/0000-0001-9757-6150
Ardabil University of Medical Sciences · IRIsfahan University of Technology · IRIslamic Azad University Medical Branch of Tehran · IRUniversity of Isfahan · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer is the main cause of human death due to cancer. This fact could be due to the insufficiency of early diagnosis or poor therapeutic strategies. Various molecular tools have been utilized in studies to assess their potentials as diagnostic biomarkers or determining factors in precision medicine. Among these molecules, long non-coding RNAs (lncRNA) have been emerging as accurate and potent transcripts to improve the detection of cancer. The overexpressed lncRNAs could also be deeply studied as the molecules for the targeted therapy in different malignancies, in particular colorectal cancer. Thus, we utilized an unbiased approach to select the up-regulated lncRNAs in colon adenocarcinoma via analyzing the TCGA dataset. Then, we validated the overexpression of two first-ranked lncRNAs, i.e., NPSR1-AS1 and TLX1NB, in our in-house colorectal cancer samples as compared to the paired adjacent normal tissues. The analyses revealed that these lncRNAs could significantly distinguish the tumor against the normal samples. The results may have implications in the early diagnosis and targeted therapy of colorectal cancer.

Indexed as

AdenocarcinomaBiomarkers, TumorColorectal NeoplasmsDatasets as TopicEarly Detection of CancerGene ExpressionHomeodomain ProteinsHumansMolecular Targeted TherapyProto-Oncogene ProteinsReceptors, G-Protein-CoupledRNA, Long NoncodingBiomarkers, TumorHomeodomain ProteinsNPSR1 protein, humanProto-Oncogene ProteinsReceptors, G-Protein-CoupledRNA, Long NoncodingTLX1 protein, humanColorectal cancerDiagnosisLong non-coding RNANPSR1-AS1TLX1NB

Identifiers

PMID34406628
OpenAlexW3194500244

What OpenQuestion holds

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Registered trials

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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.