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Identification of PAQR3 as a new candidate tumor suppressor in hepatocellular carcinoma
Hong Ge Wu1, Wen Jie Zhang2, Qian Ding1
1Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430023, P.R. China.
Abstract:
Progestin and adipoQ receptor family member III (PAQR3) is a regulator that negatively modulates the Ras/Raf/MEK/ERK signaling cascade and the GPCR Gβγ subunit signaling pathway. The role of PAQR3 in hepatocellular carcinoma (HCC) has not been elucidated. The present study investigated the expression of PAQR3 and its prognostic value in primary HCC patients. Furthermore, the functional aspects of PAQR3 were also studied using an in vitro cell model. PAQR3 expression was examined in paired HCC and adjacent noncancerous tissues using real-time quantitative RT-PCR (62 pairs) and western blotting (26 pairs). We also analyzed PAQR3 expression in 132 additional HCC samples by immunohistochemistry. The functional impact of PAQR3 on the proliferation and colony formation of an HCC cell line was analyzed by transfecting cells with a full-length PAQR3 expression vector or siRNA targeting PAQR3. The expression of PAQR3 was significantly decreased in the cancer tissues. Clinicopathological analyses showed that the expression of PAQR3 was significantly correlated with expression of serum α-fetoprotein (AFP), mitotic count, tumor size, histological grade and recurrence. Notably, Kaplan-Meier survival curves revealed a correlation between decreased expression of PAQR3 and the poor prognosis of HCC patients. Multivariate analyses showed that PAQR3 expression is an independent prognostic marker for overall and disease-free survival of HCC patients. Furthermore, restoring PAQR3 expression in HCC cells significantly diminished Hep3B cell proliferation and colony formation. Silencing PAQR3 expression in hepatic normal cell line LO2 significantly enhanced cell growth. PAQR3 may play an important role in the progression of HCC and serve as a potential candidate for the targeted therapy of HCC.
Insights
Progestin and adipoQ receptor family member III (PAQR3) is downregulated in hepatocellular carcinoma (HCC), correlating with poor prognosis. Restoring PAQR3 inhibits HCC cell growth, suggesting its therapeutic potential.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- Hepatocellular carcinoma (HCC) is a major global health concern with limited therapeutic options.
- The role of Progestin and adipoQ receptor family member III (PAQR3) in HCC progression remains unclear.
- PAQR3 is known to modulate Ras/Raf/MEK/ERK and GPCR signaling pathways.
Purpose of the Study:
- To investigate the expression and prognostic significance of PAQR3 in HCC.
- To elucidate the functional role of PAQR3 in HCC cell proliferation and growth.
- To explore PAQR3 as a potential therapeutic target for HCC.
Main Methods:
- PAQR3 expression analysis in HCC tissues and cell lines using RT-qPCR, Western blotting, and immunohistochemistry.
- Functional studies involving PAQR3 overexpression and knockdown in HCC cell lines (Hep3B) and normal liver cells (LO2).
- Correlation analysis between PAQR3 expression and clinicopathological features, including serum AFP, mitotic count, tumor size, grade, and recurrence.
Main Results:
- PAQR3 expression was significantly decreased in HCC tissues compared to adjacent noncancerous tissues.
- Reduced PAQR3 expression correlated with advanced tumor characteristics (larger size, higher grade, increased mitotic count, elevated AFP) and poorer patient prognosis.
- PAQR3 overexpression suppressed HCC cell proliferation and colony formation, while PAQR3 knockdown enhanced normal liver cell growth.
Conclusions:
- PAQR3 is downregulated in HCC and acts as an independent prognostic marker for patient survival.
- PAQR3 exhibits tumor-suppressive functions in HCC by inhibiting cell proliferation.
- PAQR3 represents a promising therapeutic target for HCC treatment.
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