Absolute quantitative PCR for detection of molecular biomarkers in melanoma patients: A preliminary report
Autor: | Mm Lavieri, Chiara Autilio, Francesca Vendittelli, Ettore Capoluongo, Rodolfo Capizzi, Carmela Paolillo, Sl Silveri |
---|---|
Přispěvatelé: | Vendittelli, F., Paolillo, C., Autilio, C., Lavieri, M. M., Silveri, S. L., Capizzi, R., Capoluongo, E. |
Rok vydání: | 2015 |
Předmět: |
Adult
Male Oncology medicine.medical_specialty Pathology ATP Binding Cassette Transporter Subfamily B Skin Neoplasms Clinical Biochemistry CD146 Antigen Real-Time Polymerase Chain Reaction Biochemistry Transforming Growth Factor beta2 Circulating tumor cell Absolute qRT-PCR Preliminary report Cell Line Tumor Internal medicine Gene expression Biomarkers Tumor medicine Humans Paired Box Transcription Factors ATP Binding Cassette Transporter Subfamily B Member 1 Multimarker assay Melanoma PAX3 Transcription Factor P-glycoprotein biology business.industry Biochemistry (medical) Circulating tumor cells ABCB5 Melanoma molecular biomarker General Medicine Middle Aged medicine.disease Phenotype Real-time polymerase chain reaction biology.protein Female Settore MED/35 - MALATTIE CUTANEE E VENEREE business |
Zdroj: | Clinica Chimica Acta. 444:242-249 |
ISSN: | 0009-8981 |
DOI: | 10.1016/j.cca.2015.02.013 |
Popis: | Background Malignant melanoma is the most malignant tumours of skin and mucous membranes mainly due to its aggressive biological behaviour and tendency to generate early metastases. Unfortunately, the mechanisms underlying the development, progression and the expression of an aggressive melanoma phenotype still remain largely unknown. Objectives The purpose of this study was to determine whether a multi-panel of molecular transcripts can be predictive for risk of recurrent disease in malignant melanoma patients. Results Peripheral blood was collected from 31 malignant melanoma patients in follow-up for melanoma and from 30 healthy volunteers randomly selected. Each specimen was examined by qRT-PCR analysis for the expression of six markers: PAX3d, TYR, MITFm, MCAM, TGFβ2 and ABCB5. Malignant melanoma patients expressed an important number of markers, with a median value of four markers. Only PAX3d displayed a trend in terms of differences when the levels of gene expression were made in function of Breslow index. Furthermore, PAX3d showed the best diagnostic capacity among the remaining residual markers or in combination with TGFβ2 and MTIF. Conclusions We demonstrated the usefulness of multimarker qRT-PCR to detect circulating melanoma cells in blood and to potentially assessing patient disease status or progression, especially when PAX3d was used in combination with MTIFm and TGFβ2. |
Databáze: | OpenAIRE |
Externí odkaz: |