Cancer genetics · 2025
Expression and clinical significance of the imprinted gene PHLDA2 in colorectal cancer.
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Li Haohui, Jin Chenting, Zhou Fangfang, Bao Man, Tan Canliang, Luo Zhenchao, Li Ninglei, Jin Yiyi, Han Luzhe, Xiao Gang, Yan Jian
Аннотация
BACKGROUND: Colorectal cancer (CRC) is one of the most prevalent malignancies worldwide and a leading cause of cancer-related mortality. Tumor progression and metastasis, particularly to the lymph nodes, are critical factors contributing to poor patient outcomes. Identifying molecular markers that predict disease progression and patient survival is essential for improving CRC prognosis and therapeutic strategies.
OBJECTIVE: This study aims to investigate the clinical significance of PHLDA2 expression in CRC and its potential as a prognostic marker.
METHODS: PHLDA2 expression levels in CRC tissues were analyzed using Oncomine database and validated through immunohistochemistry. Mean optical density (MOD) scores were used to quantify PHLDA2 protein expression, and mRNA levels were analyzed in tissue samples. Kaplan-Meier survival analysis was performed to determine the effect of PHLDA2 expression on overall survival (OS). The impact of PHLDA2 on CRC cell behavior was examined by knocking out PHLDA2 in HCT 116 and DLD-1 cell lines, followed by assessments of cell proliferation, migration, invasion, and colony formation in vitro. Additionally, the effects of PHLDA2 knockout were evaluated in xenograft models.
RESULTS: PHLDA2 expression was significantly upregulated in CRC tissues compared to adjacent normal tissues. Elevated PHLDA2 levels were associated with lymph node metastasis, with a high expression in 69.23% of rectal cancer patients with metastasis compared to 33.33% in those without metastasis (p = 0.0363). Patients with higher PHLDA2 expression (2+/3+) had significantly worse OS than those with low or no expression (p < 0.05). Functional assays revealed that PHLDA2 knockout significantly reduced proliferation, migration, invasion, and colony formation in HCT 116 and DLD-1 cells. In vivo, PHLDA2 knockout markedly decreased tumor growth in xenograft models.
CONCLUSIONS: Increased PHLDA2 expression is associated with more advanced CRC, particularly in cases with lymph node metastasis, and is linked to poorer survival outcomes. These findings suggest that PHLDA2 may be a valuable prognostic marker in CRC.
OBJECTIVE: This study aims to investigate the clinical significance of PHLDA2 expression in CRC and its potential as a prognostic marker.
METHODS: PHLDA2 expression levels in CRC tissues were analyzed using Oncomine database and validated through immunohistochemistry. Mean optical density (MOD) scores were used to quantify PHLDA2 protein expression, and mRNA levels were analyzed in tissue samples. Kaplan-Meier survival analysis was performed to determine the effect of PHLDA2 expression on overall survival (OS). The impact of PHLDA2 on CRC cell behavior was examined by knocking out PHLDA2 in HCT 116 and DLD-1 cell lines, followed by assessments of cell proliferation, migration, invasion, and colony formation in vitro. Additionally, the effects of PHLDA2 knockout were evaluated in xenograft models.
RESULTS: PHLDA2 expression was significantly upregulated in CRC tissues compared to adjacent normal tissues. Elevated PHLDA2 levels were associated with lymph node metastasis, with a high expression in 69.23% of rectal cancer patients with metastasis compared to 33.33% in those without metastasis (p = 0.0363). Patients with higher PHLDA2 expression (2+/3+) had significantly worse OS than those with low or no expression (p < 0.05). Functional assays revealed that PHLDA2 knockout significantly reduced proliferation, migration, invasion, and colony formation in HCT 116 and DLD-1 cells. In vivo, PHLDA2 knockout markedly decreased tumor growth in xenograft models.
CONCLUSIONS: Increased PHLDA2 expression is associated with more advanced CRC, particularly in cases with lymph node metastasis, and is linked to poorer survival outcomes. These findings suggest that PHLDA2 may be a valuable prognostic marker in CRC.