2018
DOI: 10.3892/ijmm.2018.3985
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Overexpression of CDCA8 promotes the malignant progression of cutaneous melanoma and leads to poor prognosis

Abstract: Cutaneous melanoma is very aggressive and results in high mortality rates for cancer patients. Determining molecular targets is important for developing novel therapies for cutaneous melanoma. Cell division cycle associated 8 (CDCA8) is a putative oncogene that is upregulated in multiple types of cancer. The present study aimed to examine the role of CDCA8 in cutaneous melanoma, with a focus on the association of its expression to prognosis and metastasis. First, the mRNA expression of CDCA8 in cutaneous melan… Show more

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Cited by 57 publications
(64 citation statements)
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“…Previous study revealed that CDCA8 was overexpressed in colorectal cancers and that loss of CDCA8 suppressed the growth of cancer cells and induced apoptosis . Furthermore, it was reported that high expression of CDCA8 was significantly associated with lymph node metastasis in melanoma . CDCA8, therefore, may work as a promoter in lymph node metastasis of PCa and have the potential to become a novel diagnostic and therapeutic factor for PCa.…”
Section: Discussionmentioning
confidence: 98%
“…Previous study revealed that CDCA8 was overexpressed in colorectal cancers and that loss of CDCA8 suppressed the growth of cancer cells and induced apoptosis . Furthermore, it was reported that high expression of CDCA8 was significantly associated with lymph node metastasis in melanoma . CDCA8, therefore, may work as a promoter in lymph node metastasis of PCa and have the potential to become a novel diagnostic and therapeutic factor for PCa.…”
Section: Discussionmentioning
confidence: 98%
“…With regard to renal cancer, CDCA8 has also certain prognostic value [53]. CDCA8 promotes the malignant progression of cutaneous melanoma [54]. Furthermore, CDCA8 also exerts a vital part during lung carcinogenesis [55].…”
Section: Discussionmentioning
confidence: 99%
“…In order to explore the specific mechanism of the effect of these genes on survival, we screened the top 10 genes (CDC20, NCAPH, CDCA5, BUB1, CDCA8, PBK, KIF2C, TPX2, TTK and TOP2A). By retrieving related literature, we found that CDCA5 and CDCA8, as important regulatory proteins in the cell cycle in cancer, were recognized as oncogenes [26][27][28][29]. However, compared with other genes, there scarcely no reports about the mechanism of CDCA5 and CDCA8 with GBM.…”
Section: Discussionmentioning
confidence: 99%