Evidence map›Paper›PMID 38156838›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2023

Epigenetic Modulation of DDIT3 and MGMT Expression Acts Synergistically with Resistance to Imatinib towards CML Disease Progression: A Hospital based Study.

Gautam Hazarika, Manash Jyoti Kalita, Simanta Kalita, Partha Pratim Das, Kalpajit Dutta, Lipika Lahkar, Anjanjyoti Rajkonwar, Mohammed Ghaznavi Idris, Vinotsale Khamo, Giriraj Kusre and 1 more

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 25% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 4 institutions in 1 country.

Gautam HazarikaDepartment of Anatomy, Assam Medical College &Hospital, Dibrugarh, (Assam) India.
Manash Jyoti KalitaDepartment of Bioengineering & Technology, Gauhati University, Guwahati, (Assam) India.
Simanta KalitaDepartment of Bioengineering & Technology, Gauhati University, Guwahati, (Assam) India.
Partha Pratim DasDepartment of Bioengineering & Technology, Gauhati University, Guwahati, (Assam) India.ORCID 0000-0001-6239-3952
Kalpajit DuttaDepartment of Bioengineering & Technology, Gauhati University, Guwahati, (Assam) India.ORCID 0000-0002-8586-112X
Lipika LahkarDepartment. of Botany, Silapathar College, Dhemaji, (Assam) India.
Anjanjyoti RajkonwarDepartment of Anatomy, Assam Medical College &Hospital, Dibrugarh, (Assam) India.
Mohammed Ghaznavi IdrisDepartment of Bioengineering & Technology, Gauhati University, Guwahati, (Assam) India.
Vinotsale KhamoDepartment of Pathology, Naga Hospital Authority, Kohima, (Nagaland) India.
Giriraj KusreDepartment of Anatomy, Assam Medical College &Hospital, Dibrugarh, (Assam) India.
Subhash MedhiDepartment of Bioengineering & Technology, Gauhati University, Guwahati, (Assam) India.ORCID 0000-0002-2733-8293
Gauhati University · INAssam Medical College · INNagaland University · INSilchar Medical College and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImatinib Mesylate is an authenticated drug that aids in the treatment of Chronic Myeloid Leukaemia and Philadelphia patients which is recognized as a BCR-ABL tyrosine kinase inhibitor. Indeed, DNA Methylation occupies a key role in the stability of chromosomes.

objectiveChanges in the methylation status of genes may impart to the advancement of Chronic Myeloid Leukaemia. The present investigation aims to assess the role of expression analysis and methylation status of DDIT3 and MGMT genes in imatinib-resistant and nonresistant cases.

methodsThe Imatinib resistance was screened through RFLP. In this case maximum number of patients were recorded in the chronic phase belonging to the age group 40-59 and the accelerated and blast phase is more common in elderly patients showing the progressive nature of the disease with age. Hemoglobin and platelet count are found to be higher in cases where WBC count was minimal. A history of long-term alcohol consumption is found to be associated with the progression of the disease.

resultsThe maximum level of expression of the DDIT3 gene was recorded in the chronic phase regardless of upstream (67.8%) and downstream (57.9%) regulation. The highest MGMT expression regulation was also observed in the case of chronic phase in both upstream (78.9%) and downstream (44%) regulation. Further, the MGMT gene showed the highest methylation of 6.6% and DDIT3 showed 3.3% in CML cases.

conclusionIn the present study notable depletion of survivality was established in the Imatinib resistance patients manifesting genetic malfunction of BCR-ABL transcripts among the North East Indian inhabitants and advocating for the expansion of the disease.

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositivePyrimidinesAgedDisease ProgressionDNA Modification MethylasesDNA Repair EnzymesDrug Resistance, NeoplasmEpigenesis, GeneticFusion Proteins, bcr-ablHumansImatinib MesylateProtein Kinase InhibitorsTranscription Factor CHOPTumor Suppressor ProteinsDDIT3 protein, humanDNA Modification MethylasesDNA Repair EnzymesFusion Proteins, bcr-ablImatinib MesylateMGMT protein, humanProtein Kinase InhibitorsPyrimidinesTranscription Factor CHOPTumor Suppressor ProteinsChronic myeloid leukemiaDDIT3 and MGMTDNA MethylationImatinib Resistant

Identifiers

PMID38156838
PMCPMC10909112
OpenAlexW4390399096

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.