Marcello Filotico
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Marcello Filotico has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Blas Flor-Lorente
Digestive Surgery Department, "La Fe" University Hospital, Valencia, Spain
1 shared publication - Daniela Rega
Colorectal Surgical Oncology, Department of Abdominal Oncology, Istituto Nazionale Tumori-IRCCS “Fondazione G. Pascale”, Naples, Italy
1 shared publication - Federica Di Maggio
Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80131 Naples, Italy
1 shared publication - Francesco Corcione
Clinica Mediterranea, 80122 Naples, Italy
1 shared publication - Francesco Salvatore
Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80131 Naples, Italy
1 shared publication - Giuseppe Boccia
Oncological and Minimally Invasive Surgery at Clinica Mediterranea, 80122 Naples, Italy
1 shared publication
Latest Publications
- 5 April 2024
- Published by Wiley in Colorectal Disease
- Vol. 26 (6) , 1318-1319
Incidental diagnosis and intra‐operative treatment of left paraduodenal hernia in a patient undergoing ultra‐low rectal anterior resection—a video vignette
- 5 April 2024
- Published by Wiley in Colorectal Disease
- Vol. 26 (6) , 1318-1319
Incidental diagnosis and intra‐operative treatment of left paraduodenal hernia in a patient undergoing ultra‐low rectal anterior resection—a video vignette
- 1 March 2024
- Published by Wiley in Colorectal Disease
- Vol. 26 (5) , 1076-1077
Perianal extramammary Paget disease: our experience of two cases – a video vignette
- 1 March 2024
- Published by Wiley in Colorectal Disease
- Vol. 26 (5) , 1076-1077
Perianal extramammary Paget disease: our experience of two cases – a video vignette
- Open Access
- 27 February 2024
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 25 (5) , 2716
A Novel DNA Variant in SMARCA4 Gene Found in a Patient Affected by Early Onset Colon Cancer
Colorectal cancer is the third leading cause of death from neoplasia worldwide. Thanks to new screening programs, we are now seeing an increase in Early Onset of ColoRectal Cancer (EOCRC) in patients below the age of 50. Herein, we report a clinical case of a woman affected by EOCRC. This case illustrates the importance of genetic predisposition testing also in tumor patients. Indeed, for our patient, we used a combined approach of multiple molecular and cellular biology technologies that revealed the presence of an interesting novel variant in the SMARCA4 gene. The latter gene is implicated in damage repair processes and related, if mutated, to the onset of various tumor types. In addition, we stabilized Patient-Derived Organoids from the tumor tissue of the same patient and the result confirmed the presence of this novel pathogenic variant that has never been found before even in early onset cancer. In conclusion, with this clinical case, we want to underscore the importance of including patients even those below the age of 50 years in appropriate screening programs which should also include genetic tests for predisposition to early onset cancers.
- 27 February 2024
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 25 (5) , 2716
Open AccessA Novel DNA Variant in SMARCA4 Gene Found in a Patient Affected by Early Onset Colon Cancer
Colorectal cancer is the third leading cause of death from neoplasia worldwide. Thanks to new screening programs, we are now seeing an increase in Early Onset of ColoRectal Cancer (EOCRC) in patients below the age of 50. Herein, we report a clinical case of a woman affected by EOCRC. This case illustrates the importance of genetic predisposition testing also in tumor patients. Indeed, for our patient, we used a combined approach of multiple molecular and cellular biology technologies that revealed the presence of an interesting novel variant in the SMARCA4 gene. The latter gene is implicated in damage repair processes and related, if mutated, to the onset of various tumor types. In addition, we stabilized Patient-Derived Organoids from the tumor tissue of the same patient and the result confirmed the presence of this novel pathogenic variant that has never been found before even in early onset cancer. In conclusion, with this clinical case, we want to underscore the importance of including patients even those below the age of 50 years in appropriate screening programs which should also include genetic tests for predisposition to early onset cancers.