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Expression of Melanoma Antigen Genes A11 and A12 in Non-Small Cell Lung Cancer

Authors :
Gondo Mastutik
Alphania Rahniayu
Isnin Anang Marhana
Mochamad Amin
Heru Fajar Trianto
Reny I'tishom
Gondo Mastutik
Alphania Rahniayu
Isnin Anang Marhana
Mochamad Amin
Heru Fajar Trianto
Reny I'tishom
Source :
Folia Medica Indonesiana; Vol. 59 No. 4 (2023): December; 363-369; 2599-056X; 2355-8393
Publication Year :
2023

Abstract

Highlights:1. In this study, new primers designed using the semi-nested polymerase chain reaction (PCR) method were utilized to identify MAGE-A11 and MAGE-A12 expressions in specimens collected from core biopsy, forcep biopsy, and bronchoalveolar lavage. 2. The histopathological analysis revealed positive expressions of MAGE-A11 and MAGE-A12 in specimens diagnosed with non-small cell lung cancer (NSCLC) as well as in specimens with no malignant cells. 3. This study provides evidence indicating that the detection of messenger ribonucleic acid (mRNA) of MAGE-A11 and MAGE-A12 by nested reverse transcription PCR can improve the accuracy of lung cancer diagnosis. AbstractThe melanoma antigen gene (MAGE) belongs to the group of cancer-testis antigens that are exclusively expressed in germ cells but may be re-expressed in cancer cells. The highly expressed MAGE-A subfamily in lung cancer may potentially be a diagnostic and prognostic biomarker. This study aimed to identify MAGE-A11 and MAGE-A12 expressions in lung tumors obtained from core biopsy, forceps biopsy, and bronchoalveolar lavage specimens. A cross-sectional observational study was conducted on 90 patients clinically diagnosed with lung tumors. These patients received core biopsy, forceps biopsy, and bronchoalveolar lavage interventions after ethical approval was obtained. The complementary deoxyribonucleic acid (cDNA) quality was assessed by the polymerase chain reaction (PCR) of glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The assessment was performed to ascertain if all specimens exhibited positive PCR amplification of the GAPDH gene. MAGE-A11 and MAGE-A12 were identified through a semi-nested reverse transcription PCR. The positive results were detected by measuring the PCR products, with MAGE-A11 and MAGE-A12 at base pairs (bp) of 858 and 496 in the first and second rounds, respectively. The expressions of MAGE-A11 and MAGE-A12 were observed in 3 (3.33%) and 40 (44.44%) out of 90 specimens, respective

Details

Database :
OAIster
Journal :
Folia Medica Indonesiana; Vol. 59 No. 4 (2023): December; 363-369; 2599-056X; 2355-8393
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1417052389
Document Type :
Electronic Resource