Periostin, tenascin, osteopontin isoforms in long- and non-long survival patients with pancreatic cancer: a pilot study.
Adenocarcinoma
/ metabolism
Adult
Cell Adhesion Molecules
/ biosynthesis
Disease-Free Survival
Female
Humans
Male
Middle Aged
Neoplasm Proteins
/ biosynthesis
Osteopontin
/ biosynthesis
Pancreatic Neoplasms
/ metabolism
Pilot Projects
Protein Isoforms
/ biosynthesis
Survival Rate
Tenascin
/ biosynthesis
Cancer
Gene expression
Matricellular proteins
Pancreatic adenocarcinoma
Survival
mRNA
Journal
Molecular biology reports
ISSN: 1573-4978
Titre abrégé: Mol Biol Rep
Pays: Netherlands
ID NLM: 0403234
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
10
05
2020
accepted:
28
08
2020
pubmed:
5
9
2020
medline:
21
5
2021
entrez:
5
9
2020
Statut:
ppublish
Résumé
Pancreatic adenocarcinoma (PDAC) is the most frequent histological type of malignancy in the pancreas. Extracellular matrix (ECM), plays a critical role during the process of human carcinogenesis and the possible diversity in matricellular proteins composition of ECM may have a significant impact on the clinical course of PDAC. Aim of this paper was to evaluate the expression of three matricellular proteins, including Periostin (POSTN), Tenascin (TNS) and Osteopontin (OPN), in PDAC from long-survival (LS) and non-long survival (NLS) patients. A total of 30 PDAC were analyzed, 15 from patients that survived more than 60 months after surgery (LS) and 15 that died from the disease within 24 (NLS). RNA was extracted and OPN, TNS and POSTN mRNA levels were evaluated by qRT-PCR. LS and NLS samples showed the same type of POSTN and TN isoforms. On the contrary, OPN seems to be preferentially expressed in NLS PDAC. Moreover, OPNb and OPNc isoforms were expressed exclusively in NLS samples. In conclusion, Our data led to hypothesize a possible relationship between the expression of different isoforms of each of these proteins and the clinical outcome of patients with PDAC.
Identifiants
pubmed: 32886326
doi: 10.1007/s11033-020-05763-2
pii: 10.1007/s11033-020-05763-2
doi:
Substances chimiques
Cell Adhesion Molecules
0
Neoplasm Proteins
0
POSTN protein, human
0
Protein Isoforms
0
SPP1 protein, human
0
Tenascin
0
Osteopontin
106441-73-0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM