Evidence map›Paper›PMID 34958000›Full record

ArticleCancer biomarkers : section A of Disease markers2022

Cytoplasmic expression of DCLK1-S, a novel DCLK1 isoform, is associated with tumor aggressiveness and worse disease-specific survival in colorectal cancer.

Elham Kalantari, Roya Ghods, Leili Saeednejad Zanjani, Mandana Rahimi, Leila Eini, Mahdieh Razmi, Mohsen Asadi-Lari, Zahra Madjd

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

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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

11 citing papers in PubMed, 12 citations in OpenAlex.

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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.

Elham KalantariOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Roya GhodsOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Leili Saeednejad ZanjaniOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Mandana RahimiDepartment of Pathology, Hasheminejad Kidney Center, School of Medicine, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Leila EiniOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Mahdieh RazmiOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Mohsen Asadi-LariOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Zahra MadjdOncopathology Research Center, Iran University of Medical Sciences (IUMS), Tehran, Iran.
Iran University of Medical Sciences · IRIslamic Azad University, Science and Research Branch · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIsoform-specific function of doublecortin-like kinase 1 (DCLK1) has highlighted the key role of the DCLK1-S (short isoform) in the maintenance, progression, and invasion of the tumor.

objectiveThis study was designed to produce an anti-DCLK1-S polyclonal antibody to evaluate DCLK1-S in human colorectal cancer (CRC) specifically.

methodsThe expression pattern and clinical significance of DCLK1-S were assessed in a well-defined tissue microarray (TMA) series of 348 CRC and 51 adjacent normal tissues during a follow-up period of 108 months.

resultsExpression of DCLK1-S was significantly higher in CRC samples compared to adjacent normal samples (P< 0.001). Cytoplasmic expression of DCLK1-S was significantly higher in the tumors at the advanced stage of cancer and with poorer differentiation (P< 0.001, P= 0.02). The patients with CRC whose tumors showed higher cytoplasmic expression of DCLK1-S had worse disease-specific survival (DSS) (log-rank test, P= 0.03) and 5-year DSS rates (P= 0.01). Additionally, an improved prognostic value was observed in the patients with CRC with high DCLK1-S expression vs. its moderate expression (HR: 2.70, 95% CI: 0.98-7.38; p= 0.04) by multivariate analysis.

conclusionsOur findings strongly supported that high cytoplasmic expression of DCLK1-S compared to its moderate expression could be considered an independent prognostic factor influencing DSS.

Indexed as

Colorectal NeoplasmsDoublecortin-Like KinasesBiomarkers, TumorHumansIntracellular Signaling Peptides and ProteinsProtein IsoformsProtein Serine-Threonine KinasesBiomarkers, TumorDCLK1 protein, humanDoublecortin-Like KinasesIntracellular Signaling Peptides and ProteinsProtein IsoformsProtein Serine-Threonine KinasesColorectal cancerDCLK1-Simmunohistochemistrypolyclonal antibodytissue microarray

Identifiers

PMID34958000
PMCPMC12364155
OpenAlexW4225357253

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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.