2009•PubMedRequires access

[Impact of PrLZ overexpression on invasion of prostate cancer LNCaP cells in vitro].

Dong Zhang, Lei Li, Linlin Zhang, Yan Xue, Xinyang Wang, Dalin He

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Abstract

BACKGROUND AND OBJECTIVE: Prostate leucine zipper (PrLZ), a novel gene, is highly associated with the malignant progression of prostate cancer. We previously found that PrLZ overexpression can enhance the survival of prostate cancer LNCaP cells in vitro. This study was to investigate the impact of PrLZ on the invasion of LNCaP cells and its possible mechanism. METHODS: PrLZ was transfected into LNCaP cells. LNCaP/PrLZ cells with high expression of PrLZ were screened with G418. The migration and invasion of LNCaP and LNCaP/PrLZ cells were detected by Transwell assay. The level and activity of matrix metalloproteinase-2 (MMP-2) was determined by Western blot and Zymography, respectively. RESULTS: Migration cell count of LNCaP and LNCaP/PrLZ cells were 64.8+/-8.7 and 69.3+/-7.6, respectively (P>0.05), whereas invasive cell count of LNCaP and LNCaP/PrLZ cells were 70.7+/-2.8 and 190.5+/-9.3, respectively (P<0.001). Both the expression and activity of MMP-2 in LNCaP/PrLZ cells were enhanced. CONCLUSION: PrLZ may be involved in the invasion of prostate cancer.

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What this paper is about

BACKGROUND AND OBJECTIVE: Prostate leucine zipper (PrLZ), a novel gene, is highly associated with the malignant progression of prostate cancer. We previously found that PrLZ overexpression can enhance the survival of prostate cancer LNCaP cells in vitro. This study was to investigate the impact of PrLZ on the invasion of LNCaP cells and its possible mechanism. METHODS: PrLZ was transfected into LNCaP cells. LNCaP/PrLZ cells with high expression of PrLZ were screened with G418. The migration and invasion of LNCaP and LNCaP/PrLZ cells were detected by Transwell assay. The level and activity of matrix metalloproteinase-2 (MMP-2) was determined by Western blot and Zymography, respectively. RESULTS: Migration cell count of LNCaP and LNCaP/PrLZ cells were 64.8+/-8.7 and 69.3+/-7.6, respectively (P>0.05), whereas invasive cell count of LNCaP and LNCaP/PrLZ cells were 70.7+/-2.8 and 190.5+/-9.3, respectively (P<0.001). Both the expression and activity of MMP-2 in LNCaP/PrLZ cells were enhanced. CONCLUSION: PrLZ may be involved in the invasion of prostate cancer.

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Available abstract

BACKGROUND AND OBJECTIVE: Prostate leucine zipper (PrLZ), a novel gene, is highly associated with the malignant progression of prostate cancer. We previously found that PrLZ overexpression can enhance the survival of prostate cancer LNCaP cells in vitro. This study was to investigate the impact of PrLZ on the invasion of LNCaP cells and its possible mechanism. METHODS: PrLZ was transfected into LNCaP cells. LNCaP/PrLZ cells with high expression of PrLZ were screened with G418. The migration and invasion of LNCaP and LNCaP/PrLZ cells were detected by Transwell assay. The level and activity of matrix metalloproteinase-2 (MMP-2) was determined by Western blot and Zymography, respectively. RESULTS: Migration cell count of LNCaP and LNCaP/PrLZ cells were 64.8+/-8.7 and 69.3+/-7.6, respectively (P>0.05), whereas invasive cell count of LNCaP and LNCaP/PrLZ cells were 70.7+/-2.8 and 190.5+/-9.3, respectively (P<0.001). Both the expression and activity of MMP-2 in LNCaP/PrLZ cells were enhanced. CONCLUSION: PrLZ may be involved in the invasion of prostate cancer.

Key concepts: LNCaP, Prostate cancer, Gentamicin protection assay, Transfection, Cancer research, Cancer cell, Matrix metalloproteinase, Biology

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[Impact of PrLZ overexpression on invasion of prostate cancer LNCaP cells in vitro]. — Research Paper | ScholarLens