Evidence map›Paper›PMID 33082414›Full record

ArticleScientific reports2020

Low expression of Talin1 is associated with advanced pathological features in colorectal cancer patients.

Somayeh Vafaei, Leili Saeednejad Zanjani, Zohreh Habibi Shams, Marzieh Naseri, Fahimeh Fattahi, Elmira Gheytanchi, Mahdi Alemrajabi, Marzieh Ebrahimi, Zahra Madjd

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

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  13. Prognostic value of Talin-1 in renal cell carcinoma and its association with B7-H3.Cancer biomarkers : section A of Disease markers · 2022
    Article
  14. Article
  15. Expression of Talin-1 in endometriosis and its possible role in pathogenesis.Reproductive biology and endocrinology : RB&E · 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

9 authors at 4 institutions in 1 country.

Somayeh VafaeiOncopathology Research Center, Iran University of Medical Sciences (IUMS), Hemmat Street (Highway), Next To Milad Tower, Tehran, Iran.
Leili Saeednejad ZanjaniOncopathology Research Center, Iran University of Medical Sciences (IUMS), Hemmat Street (Highway), Next To Milad Tower, Tehran, Iran.
Zohreh Habibi ShamsDepartment of Pathology, Iran University of Medical Sciences, Tehran, Iran.
Marzieh NaseriOncopathology Research Center, Iran University of Medical Sciences (IUMS), Hemmat Street (Highway), Next To Milad Tower, Tehran, Iran.
Fahimeh FattahiDepartment of Molecular Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
Elmira GheytanchiOncopathology Research Center, Iran University of Medical Sciences (IUMS), Hemmat Street (Highway), Next To Milad Tower, Tehran, Iran.
Mahdi AlemrajabiFiroozgar Clinical Research Development Center, Firoozgar Hospital (FCRDC), Iran University of Medical Sciences (IUMS), Tehran, Iran.
Marzieh EbrahimiDepartment of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, 16635-148, Tehran, Iran. mebrahimi@royaninstitute.org.
Zahra MadjdOncopathology Research Center, Iran University of Medical Sciences (IUMS), Hemmat Street (Highway), Next To Milad Tower, Tehran, Iran. majdjabari.z@iums.ac.ir.
Iran University of Medical Sciences · IRAcademic Center for Education, Culture and Research · IRFiroozgar General Hospital · IRRoyan Institute · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To explore the proper prognostic markers for the likelihood of metastasis in CRC patients. Seventy-seven fresh CRC samples were collected to evaluate the mRNA level of the selected marker using Real-time PCR. Moreover, 648 formalin-fixed paraffin-embedded CRC tissues were gathered to evaluate protein expression by immunohistochemistry (IHC) on tissue microarrays. The results of Real-Time PCR showed that low expression of Talin1 was significantly associated with advanced TNM stage (p = 0.034) as well as gender (p = 0.029) in mRNA levels. Similarly, IHC results indicated that a low level of cytoplasmic expression of Talin1 was significantly associated with advanced TNM stage (p = 0.028) as well as gender (p = 0.009) in CRC patients. Moreover, decreased expression of cytoplasmic Talin1 protein was found to be a significant predictor of worse disease-specific survival (DSS) (p = 0.011) in the univariate analysis. In addition, a significant difference was achieved (p = 0.039) in 5-year survival rates of DSS: 65% for low, 72% for moderate, and 88% for high Talin1 protein expression. Observations showed that lower expression of Talin1 at both the gene and protein level may drive the disparity of CRC patients' outcomes via worse DSS and provide new insights into the development of progression indicators because of its correlation with increased tumor aggressiveness.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinogenesisColonic NeoplasmsColorectal NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm StagingPredictive Value of TestsPrognosisSurvival AnalysisBiomarkers, TumorTalinTLN1 protein, human

Identifiers

PMID33082414
PMCPMC7576823
OpenAlexW3094227211

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.