TY - JOUR
T1 - p53 expression is associated with tumor stage, grade and subtype in patients with hepatocellular carcinoma
AU - Rahadiani, Nur
AU - Stephanie, Marini
AU - Perkasa, Alif Gilang
AU - Handjari, Diah Rini
AU - Krisnuhoni, Ening
N1 - Funding Information:
The present study was funded by the Ministry of Research and Technology/National Agency for Research and Innovation through the Research and Community Service Information System (SIMLITABMAS/BRIN) grant and the Top Basic Research in University (PDUPT) scheme (grant no. NKB‑121, year 2021).
Publisher Copyright:
© 2023 Rahadiani et al.
PY - 2023
Y1 - 2023
N2 - The present study aimed to determine the expression levels of p53 in patients with hepatocellular carcinoma (HCC) and to evaluate its association with several HCC-related prognostic factors and in particular, with tumor stage, grade and subtype. Therefore, a cross-sectional study, involving 41 patients with HCC, who underwent surgical resection between January, 2013 and December, 2020 was conducted. To assess the expression levels of p53 in all patients with HCC, immunohistochemical staining was performed. In addition, the association between p53 expression and the clinico-pathological characteristics of patients with HCC, including prognostic factors, was evaluated by applying the appropriate statistical analysis methods. The results revealed that among the 41 patients enrolled, 35 patients (85.4%) were positive for p53 expression. A higher percentage of positive p53 expression was observed in male patients >60 years old, with single HCC nodules >5 cm in diameter and vascular invasion, compared with their counterparts. A positive p53 expression was associated with well- and poorly differentiated HCC, but not with tumor stage and subtype. No differences in p53 expression were observed across different tumor stages and subtypes. Additionally, patients with moderately and poorly differentiated HCC exhibited significantly higher p53 expression levels compared with those suffering from well-differentiated HCC. Overall, the results demonstrated that the rate of p53 immuno-positive cells was increased in patients with HCC. In addition, p53 expression was associated with well- and poorly differentiated HCC, thus suggesting its association with a poorer prognosis.
AB - The present study aimed to determine the expression levels of p53 in patients with hepatocellular carcinoma (HCC) and to evaluate its association with several HCC-related prognostic factors and in particular, with tumor stage, grade and subtype. Therefore, a cross-sectional study, involving 41 patients with HCC, who underwent surgical resection between January, 2013 and December, 2020 was conducted. To assess the expression levels of p53 in all patients with HCC, immunohistochemical staining was performed. In addition, the association between p53 expression and the clinico-pathological characteristics of patients with HCC, including prognostic factors, was evaluated by applying the appropriate statistical analysis methods. The results revealed that among the 41 patients enrolled, 35 patients (85.4%) were positive for p53 expression. A higher percentage of positive p53 expression was observed in male patients >60 years old, with single HCC nodules >5 cm in diameter and vascular invasion, compared with their counterparts. A positive p53 expression was associated with well- and poorly differentiated HCC, but not with tumor stage and subtype. No differences in p53 expression were observed across different tumor stages and subtypes. Additionally, patients with moderately and poorly differentiated HCC exhibited significantly higher p53 expression levels compared with those suffering from well-differentiated HCC. Overall, the results demonstrated that the rate of p53 immuno-positive cells was increased in patients with HCC. In addition, p53 expression was associated with well- and poorly differentiated HCC, thus suggesting its association with a poorer prognosis.
KW - hepatocellular carcinoma
KW - histologic subtype
KW - p53
KW - tumor grade
KW - tumor stage
UR - http://www.scopus.com/inward/record.url?scp=85165386829&partnerID=8YFLogxK
U2 - 10.3892/mco.2023.2650
DO - 10.3892/mco.2023.2650
M3 - Article
AN - SCOPUS:85165386829
SN - 2049-9450
VL - 19
JO - Molecular and Clinical Oncology
JF - Molecular and Clinical Oncology
IS - 1
M1 - 54
ER -