TY - JOUR
T1 - Clinicopathological features of hepatocellular carcinoma with fatty change
T2 - Tumors with macrovesicular steatosis have better prognosis and aberrant expression patterns of perilipin and adipophilin
AU - Kubota, Naoto
AU - Ojima, Hidenori
AU - Hatano, Mami
AU - Yamazaki, Ken
AU - Masugi, Yohei
AU - Tsujikawa, Hanako
AU - Nishimura, Yoko
AU - Ueno, Akihisa
AU - Kurebayashi, Yutaka
AU - Shinoda, Masahiro
AU - Kitago, Minoru
AU - Abe, Yuta
AU - Kitagawa, Yuko
AU - Sakamoto, Michiie
N1 - Funding Information:
This research was supported by AMED under Grant Number JP19fk0210040. We thank Mr. David Smallbones for copyediting a draft of this article.
Publisher Copyright:
© 2020 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd
PY - 2020/4/1
Y1 - 2020/4/1
N2 - The clinicopathological characteristics of steatosis in hepatocellular carcinoma (HCC) remain unclear. Here, we elucidate the features of macrovesicular steatosis (MaS) and microvesicular steatosis (MiS) in HCC and their relationships with background liver steatosis. A total of 165 HCC lesions were classified as MaS-HCC, MiS-HCC, or conventional HCC (cHCC) according to the cutoff value of 30% MaS or MiS in tumor cells. We analyzed the clinicopathological differences among these groups. MaS-HCC had less portal vein invasion, a higher proportion of HCC with intratumoral fibrosis, and a lower cumulative risk of recurrence than MiS-HCC or cHCC. Moreover, both MaS-HCC and MiS-HCC had lower incidences of hepatitis virus infection and higher levels of HbA1c than cHCC. Background liver steatosis was also higher in MaS-HCC than in cHCC. Immunohistochemical expression of perilipin (Plin1) and adipophilin (ADRP), major proteins expressed on lipid droplet membranes, revealed that almost all lipid droplets in HCC were Plin1 negative, whereas those in background liver were positive. In contrast, ADRP was expressed on lipid droplets in both HCC and background liver. We concluded that MaS-HCC and MiS-HCC were associated with metabolic abnormalities but exhibited different biologic behaviors. Furthermore, lipid droplets in HCC were pathophysiologically different from those in background liver.
AB - The clinicopathological characteristics of steatosis in hepatocellular carcinoma (HCC) remain unclear. Here, we elucidate the features of macrovesicular steatosis (MaS) and microvesicular steatosis (MiS) in HCC and their relationships with background liver steatosis. A total of 165 HCC lesions were classified as MaS-HCC, MiS-HCC, or conventional HCC (cHCC) according to the cutoff value of 30% MaS or MiS in tumor cells. We analyzed the clinicopathological differences among these groups. MaS-HCC had less portal vein invasion, a higher proportion of HCC with intratumoral fibrosis, and a lower cumulative risk of recurrence than MiS-HCC or cHCC. Moreover, both MaS-HCC and MiS-HCC had lower incidences of hepatitis virus infection and higher levels of HbA1c than cHCC. Background liver steatosis was also higher in MaS-HCC than in cHCC. Immunohistochemical expression of perilipin (Plin1) and adipophilin (ADRP), major proteins expressed on lipid droplet membranes, revealed that almost all lipid droplets in HCC were Plin1 negative, whereas those in background liver were positive. In contrast, ADRP was expressed on lipid droplets in both HCC and background liver. We concluded that MaS-HCC and MiS-HCC were associated with metabolic abnormalities but exhibited different biologic behaviors. Furthermore, lipid droplets in HCC were pathophysiologically different from those in background liver.
KW - PAT family protein
KW - adipophilin
KW - fatty change
KW - fatty liver
KW - hepatocellular carcinoma
KW - lipid droplet
KW - macrovesicular steatosis
KW - metabolic abnormality
KW - microvesicular steatosis
KW - perilipin
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U2 - 10.1111/pin.12889
DO - 10.1111/pin.12889
M3 - Article
C2 - 31930673
AN - SCOPUS:85077865900
SN - 1320-5463
VL - 70
SP - 199
EP - 209
JO - Pathology international
JF - Pathology international
IS - 4
ER -