Evidence map›Paper›PMID 39068570›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

RNA Interference based Midkine Gene Therapy for Hepatocellular Carcinoma.

Samah Mamdouh, Fatma El-Zahraa Mohamed Khorshed, Gehan Hammad, Mona Magdy, Amr Abdelraouf, Eman Hemida, Mohamed Shemis

Abstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Samah MamdouhBiochemistry and Molecular Biology Department, Theodor Bilharz Research Institute (TBRI), Giza, Egypt.ORCID 0000-0001-5979-3189
Fatma El-Zahraa Mohamed KhorshedBiochemistry and Molecular Biology Department, Theodor Bilharz Research Institute (TBRI), Giza, Egypt.ORCID 0000-0003-0642-1239
Gehan HammadFaculty of Biotechnology, October University for Modern Sciences & Arts (MSA), Giza, Egypt.ORCID 0000-0002-3333-5005
Mona MagdyDepartment of Pathology, Theodor Bilharz Research Institute, Cairo, Egypt.ORCID 0000-0002-0738-1278
Amr AbdelraoufDepartment of Hepatobiliopancreatic Surgery, National Hepatology and Tropical Medicine Research Institute, (NHTMRI), Cairo, Egypt.ORCID 0000-0002-8363-568X
Eman HemidaFellow of Biochemistry, Obstetrics and Gynecology Hospital, Ain Shams University, Cairo, Egypt.
Mohamed ShemisBiochemistry and Molecular Biology Department, Theodor Bilharz Research Institute (TBRI), Giza, Egypt.ORCID 0000-0003-2493-7466

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) arises from hepatocytes and accounts for 90% of primary liver cancer. Reasons for HCC prognosis remaining dismal are that HCC is asymptomatic in its early stages, leading to late diagnosis, and it is markedly resistant to conventional chemo- and radiotherapy. In this study, we investigated RNA interference (RNAi)-based treatment for HCC by targeting MDK.

aimThe present study aimed to evaluate MDK serum levels as a diagnostic biomarker for HCC detection and the effect of MDK silencing by RNAi on HCC. SUBJECTS AND

methodsA total of 140 participants, including 120 patients diagnosed with HCC and 20 healthy volunteers were enrolled in this study, all patients who underwent liver resection were sampled for tumor and adjacent non-tumor liver tissues, in addition to 5 ml of blood sample. Midkine expression levels were evaluated by ELISA and by qRT-PCR. The in vitro transfection and gene knockdown efficiency of midkine by MDK-siRNA was detected by qRT-PCR and ELISA. Gene knockdown effect at the molecule level on the proliferation of HepG2 in vitro was determined by cell counting.

resultsThe results showed that the expression of MDK was significantly increased in the serum of HCC patients compared to control serum samples with P<0.001 and significant elevated expression levels of MDK in tumor tissues compared to non-tumor ones with P<0.001. It also showed that down-regulation of MDK using RNAi can significantly inhibit HepG2 cells.

conclusionMolecular targeting of MDK using RNAi interference decreases proliferation and could be a therapeutic target.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularCell ProliferationLiver NeoplasmsMidkineAdultCase-Control StudiesFemaleFollow-Up StudiesGenetic TherapyHep G2 CellsHumansMaleMiddle AgedPrognosisRNA InterferenceBiomarkers, TumorMDK protein, humanMidkineRNA, Small InterferingGene TherapyHCCMidkineRNAi

Identifiers

PMID39068570
PMCPMC11480621

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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.