Evidence map›Paper›PMID 38689296›Full record

ArticleBMC medical genomics2024

Circulating-tumour DNA methylation of HAND1 gene: a promising biomarker in early detection of colorectal cancer.

Mehrdad Shavali, Arash Moradi, Mohammad Tahmaseb, Kamal Mohammadian, Shahla Mohammad Ganji

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2024. 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
1.9field-weighted citation impact, top 15% 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, 8 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

5 authors at 3 institutions in 1 country.

Mehrdad Shavali *Department of Cell and Molecular Biology, Faculty of Biological Science, Kharazmi University, Tehran, Iran.
Arash Moradi *Department of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Shahrak-e Pajoohesh, km 15, P.O. Box 14965/161, Tehran, Tehran - Karaj Highway, Iran.
Mohammad TahmasebDepartment of Cell and Molecular Biology, Faculty of Biological Science, Kharazmi University, Tehran, Iran.
Kamal MohammadianDepartment of Radiation Oncology, Hamadan University of Medical Sciences, Hamadan, Iran.
Shahla Mohammad GanjiDepartment of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Shahrak-e Pajoohesh, km 15, P.O. Box 14965/161, Tehran, Tehran - Karaj Highway, Iran. shahla@nigeb.ac.ir.
Kharazmi University · IRNational Institute of Genetic Engineering and Biotechnology · IRHamedan University of Medical Sciences · IR

Funding

Biotechnology Found Foundation 01/16204
6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is one of the significant global health concerns with an increase in cases. Regular screening tests are crucial for early detection as it is often asymptomatic in the initial stages. Liquid biopsies, a non-invasive approach that examines biomarkers in biofluids, offer a promising future in diagnosing and screening cancer. Circulating-tumour DNA (ctDNA) is the genetic material in biofluids released into the circulatory system by cells. ctDNA is a promising marker for monitoring patients since cancer cells display distinct DNA methylation patterns compared to normal cells. The potential of our research to contribute to early detection and improved patient outcomes is significant.

aimsThe primary objective of this research project was to explore the HAND1 methylation levels in plasma ctDNA as a potential biomarker for diagnosing CRC and evaluate the methylation level of the well-established gene SPET9 to compare it with the methylation level of HAND1. MATERIALS AND

methodsPlasma samples were collected from 30 CRC patients and 15 healthy individuals, with CRC samples obtained pre-treatment. ctDNA was extracted and treated with bisulfite for methylation status assessment. Quantitative methylation-specific PCR (qMS-PCR) was performed for HAND1 and SEPT9, using β-actin (ACTB gene) as a reference. The study aims to evaluate the potential of these genes as diagnostic biomarkers for CRC, contributing to early detection and improved patient outcomes.

resultsOur study yielded significant results: 90% of CRC patients (27 out of 30) had hypermethylation in the SEPT9 gene, and 83% (25 out of 30) exhibited hypermethylation in the HAND1 gene. The methylation levels of both genes were significantly higher in CRC patients than in healthy donors. These findings underscore the potential of SEPT9 and HAND1 methylation as promising biomarkers for diagnosing CRC, potentially leading to early detection and improved patient outcomes.

conclusionThese findings highlight the potential of SEPT9 and HAND1 methylation as promising biomarkers for diagnosing CRC. However, further research and validation studies are needed to confirm these findings and to explore their clinical utility in CRC diagnosis and management.

Indexed as

Basic Helix-Loop-Helix ProteinsBiomarkers, TumorCirculating Tumor DNAColorectal NeoplasmsDNA MethylationEarly Detection of CancerAgedCase-Control StudiesFemaleHumansMaleMiddle AgedSeptinsBasic Helix-Loop-Helix ProteinsBiomarkers, TumorCirculating Tumor DNAhelix-loop-helix protein, eHANDSEPTIN9 protein, humanSeptinsColorectal CancerctDNAHAND1MethylationSEPT9

Identifiers

PMID38689296
PMCPMC11061902
OpenAlexW4396558862

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.