Evidence map›Paper›PMID 34582650›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2021

LGR5, HES1 and ATOH1 in Young Rectal Cancer Patients in Egyptian.

Heba Morsy, Ahmed Gaballah, Mohamed Samir, Vandrome Nakundi, Mohamed Shamseya, Hanan Mahrous, Abeer Ghazal, Mervat Hashish, Waleed Arafat

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

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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

3 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Heba MorsyDepartment of Human Genetics, Medical Research Institute, Alexandria, Egypt.
Ahmed GaballahDepartment of Microbiology, Medical Research Institute, Alexandria, Egypt.
Mohamed SamirDepartment of Clinical and Experimental Surgery, Medical Research Institute, Alexandria, Egypt.
Vandrome NakundiDepartment of Clinical Oncology and Nuclear Medicine, Faculty of Medicine, Alexandria University, Egypt.
Mohamed ShamseyaDepartment of Clinical and Experimental Internal Medicine, Medical Research Institute, Alexandria, Egypt.
Hanan MahrousDepartment of Human Genetics, Medical Research Institute, Alexandria, Egypt.
Abeer GhazalDepartment of Microbiology, Medical Research Institute, Alexandria, Egypt.
Mervat HashishDepartment of Human Genetics, Medical Research Institute, Alexandria, Egypt.
Waleed ArafatDepartment of Clinical Oncology and Nuclear Medicine, Faculty of Medicine, Alexandria University, Egypt.
Alexandria University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe study aimed to delineate the gene expression profile of LGR5, HES1 and ATOH1 in young Egyptian rectal cancer (RC) patients and investigate the correlation between expression profiles and clinical outcome.

methodsThe study was conducted on 30 young Egyptian RC patients. Expression study of LGR5, HES1 and ATOH1 were performed by quantitative PCR (QPCR) based on comparative Cq method after normalization to adjacent non tumor tissues and ACTB as a reference gene. Patients were followed up for assessment of response to neoadjuvant chemoradiotherapy (CRT) based on revised RECIST1.1.

resultThe study detected overexpression of LGR5 and HES1 and down-regulation of ATOH1 in human RC tissues compared to non- tumor tissues. High expression of LGR5 was correlated with more depth of tumor invasion, lymph node (LN) metastasis, advanced cTNM stage and mesorectal fascia (MRF) involvement. More prominently, high LGR5 expression level was associated with poor response to CRT. LGR5 was suggested as unfavorable prognostic biomarker for RC. Conversely, HES1 and ATOH1 expression did not show significant association with most of the studied clinical criteria nor response to CRT. Still, HES1 and ATOH1 were significantly and inversely associated with presence of mucinous component.

conclusionHigh LGR5 expression is indicative of poor prognosis among young Egyptian RC patients and is proposed as a predictive marker of resistance to neoadjuvant CRT. However, HES1 and ATOH1 expressions were not prognostic nor predictive of response to CRT. Overall, LGR5, HES1 and ATOH1 gene expression patterns among young onset RC patients, are in line with patterns encountered in older age groups.

Indexed as

Gene ExpressionAdultBasic Helix-Loop-Helix ProteinsEgyptFemaleHumansMaleNeoadjuvant TherapyPrognosisReceptors, G-Protein-CoupledRectal NeoplasmsTranscription Factor HES-1Young AdultATOH1 protein, humanBasic Helix-Loop-Helix ProteinsHES1 protein, humanLGR5 protein, humanReceptors, G-Protein-CoupledTranscription Factor HES-1cance stem cells chemotherapy prognosisGene expressionYoung colon cancer

Identifiers

PMID34582650
PMCPMC8850894
OpenAlexW3203472962

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LicenceCC BY
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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.