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Updated: Aug 17, 2025

A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
PIK3R2 predicts poor outcomes for patients with melanoma and contributes to the malignant progression via
Jianguo Wang1, Shizhong Cai2,3, Qianwei Xiong4,3
1Department of Surgery, Nanjing Pukou Central Hospital (Pukou Branch Hospital of Jiangsu Province Hospital), Nanjing, 211800, Jiangsu, People's Republic of China.
Background:
Melanoma is an aggressive form of skin cancer worldwide. Phosphoinositide-3-kinase regulatory subunit 2 (PIK3R2) exerts carcinogenic roles in various tumors. So far, the function and mechanism of PIK3R2 in melanoma are not been fully clarified.
Objective:
We aimed to clarify the role of PIK3R2 in melanoma.
Methods:
PIK3R2 expressions in melanoma clinical tissues and melanoma cells were measured using quantitative real-time PCR and Western blot. In addition, PIK3R2 expressions in different tumor stages of melanoma were determined by immunohistochemistry assay. Meanwhile, PIK3R2 function was evaluated using loss or gain-of-function assays, Cell Counting Kit-8 assay, flow cytometry, and Transwell analysis. Furthermore, PIK3R2 mechanism in melanoma was assessed by a series of rescue experiments.
Results:
PIK3R2 was highly expressed in melanoma tissues and cells, and PIK3R2 expressions were the highest in Stage IV. Functionally, PIK3R2 knockdown repressed melanoma cell proliferation, invasion, epithelial-mesenchymal transition, and facilitated cell apoptosis. Also, PIK3R2 overexpression produced an opposite trend. Mechanistically, PIK3R2 facilitated melanoma progression by activating PI3K/AKT/NF-κB pathway. Furthermore, PIK3R2 knockdown restrained the melanoma tumor growth in vivo.
Conclusions:
PIK3R2 aggravated melanoma by activating PI3K/AKT/NF-κB pathway, prompting that PIK3R2 might be a therapeutic target for melanoma.
Insights
Phosphoinositide-3-kinase regulatory subunit 2 (PIK3R2) drives melanoma progression by activating the PI3K/AKT/NF-κB pathway. Targeting PIK3R2 may offer a new therapeutic strategy for melanoma patients.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Melanoma is a significant global health concern.
- The role of Phosphoinositide-3-kinase regulatory subunit 2 (PIK3R2) in melanoma pathogenesis is not fully understood.
Purpose of the Study:
- To elucidate the function and mechanism of PIK3R2 in melanoma.
- To investigate PIK3R2 as a potential therapeutic target for melanoma.
Main Methods:
- Quantitative real-time PCR and Western blot to assess PIK3R2 expression in melanoma tissues and cells.
- Immunohistochemistry to correlate PIK3R2 expression with melanoma stage.
- In vitro and in vivo assays (loss/gain-of-function, CCK-8, flow cytometry, Transwell, xenograft model) to evaluate PIK3R2's functional impact.
- Rescue experiments to determine the underlying molecular mechanism.
Main Results:
- PIK3R2 expression is elevated in melanoma tissues and cells, correlating with advanced stage (Stage IV).
- PIK3R2 knockdown inhibits melanoma cell proliferation, invasion, and epithelial-mesenchymal transition, while promoting apoptosis.
- PIK3R2 overexpression exhibits opposite effects.
- PIK3R2 activates the PI3K/AKT/NF-κB pathway, promoting melanoma progression and tumor growth in vivo.
Conclusions:
- PIK3R2 exacerbates melanoma progression through the PI3K/AKT/NF-κB pathway.
- PIK3R2 represents a promising therapeutic target for melanoma treatment.
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