Analysis of Genetic Alterations in Tunisian Patients with Lung Adenocarcinoma
Autor: | Matteo Canale, Laura Capelli, Dhoha Dhieb, Paola Ulivi, Leila Keskes, Sara Bravaccini, Elisa Chiadini, Ilhem Yangui, Imen Belguith, Daniele Calistri, Tahya Boudawara, Rachid Jlidi, Ons Boudawara |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Male p53 Tunisia EGFR Adenocarcinoma of Lung medicine.disease_cause Article Proto-Oncogene Proteins p21(ras) 03 medical and health sciences 0302 clinical medicine medicine KRAS Anaplastic lymphoma kinase Humans Anaplastic Lymphoma Kinase Lung cancer lcsh:QH301-705.5 Aged business.industry Smoking Cancer Genetic Variation General Medicine Middle Aged medicine.disease lung adenocarcinoma ErbB Receptors 030104 developmental biology ALK lcsh:Biology (General) 030220 oncology & carcinogenesis Mutation Cancer research Adenocarcinoma Immunohistochemistry Female Tumor Suppressor Protein p53 business molecular profile Tyrosine kinase Immunostaining |
Zdroj: | Cells, Vol 8, Iss 6, p 514 (2019) Cells Volume 8 Issue 6 |
ISSN: | 2073-4409 |
Popis: | The identification of the mutations that drive lung cancer have furnished new targets for the treatment of non-small cell lung cancer (NSCLC) and led to the development of targeted therapies such as tyrosine kinase inhibitors that are used to combat the molecular changes promoting cancer progression. Furthermore, biomarkers identified from gene analysis can be used to detect early lung cancer, determine patient prognosis, and monitor response to therapy. In the present study we analyzed the molecular profile of seventy-three Tunisian patients with lung adenocarcinoma (LAD). Mutational analyses for EGFR and KRAS were performed using direct sequencing, immunohistochemistry or MassARRAY. Anaplastic lymphoma kinase (ALK) rearrangement was evaluated by immunohistochemistry using the D5F3 clone, and p53 expression was also assessed. The median age of patients at diagnosis was 61 years (range 23&ndash 82 years). Using different methodologies, EGFR mutations were found in 5.47% of patients and only exon 19 deletions &ldquo E746-A750 del&rdquo were detected. KRAS mutations were present in 9.58% of cases, while only one patient was ALK-positive. Moreover, abnormal immunostaining of p53 was detected in 56.16% of patients. In conclusion, the detected rates of EGFR and KRAS mutation and ALK rearrangement were lower than those found in European and Asian countries, whereas, abnormal p53 expression was slightly more frequent. Furthermore, given the small sample size of this study, a more comprehensive analysis of this patient set is warranted. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |