Evidence map›Paper›PMID 30431060›Full record

ArticleInternational journal of molecular medicine2019

Overexpression of CDCA8 promotes the malignant progression of cutaneous melanoma and leads to poor prognosis.

Chao Ci, Biao Tang, Dalun Lyu, Wenbei Liu, Di Qiang, Xiang Ji, Xiamin Qiu, Lei Chen, Wei Ding

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 83 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Chao CiDepartment of Dermatology, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Biao TangDepartment of Dermatology, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Dalun LyuDepartment of Burn and Plastic Surgery, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Wenbei LiuDepartment of Dermatology, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Di QiangDepartment of Dermatology, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Xiang JiDepartment of Dermatology, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Xiamin QiuDepartment of Dermatology, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Lei ChenDepartment of Burn and Plastic Surgery, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
Wei DingDepartment of Burn and Plastic Surgery, First Affiliated Hospital of Wannan Medical College, Wuhu, Anhui 241001, P.R. China.
First Affiliated Hospital of Wannan Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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 melanoma tissues was investigated using the ONCOMINE and Gene Expression Omnibus (GEO) databases. Furthermore, the relationship between the expression of CDCA8 and cutaneous melanoma patient survival was analyzed using a Kaplan‑Meier plot and Log Rank test. In addition, the effects of CDCA8 on proliferation, migration and invasion of cutaneous melanoma cell lines were investigated using reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR), Cell Counting kit‑8, colony formation assay, wound healing and Matrigel assay. Finally, the expression levels of key proteins related to the Rho‑associated coiled‑coil‑containing protein kinase (ROCK) signaling pathway were measured by western blot assay. The results demonstrated that CDCA8 was overexpressed in cutaneous melanoma tissues and cells lines compared with normal tissues, and high expression of CDCA8 was significantly associated with poorer prognosis in patients with cutaneous melanoma. In in vitro experiments, CDCA8 knockdown inhibited A375 and MV3 cell proliferation, migration and invasion. In addition, CDCA8 knockdown reduced the phosphorylation levels of ROCK1 and myosin light chain, two downstream effector proteins of the ROCK pathway. In summary, the present findings suggested that CDCA8 may be a promising therapeutic target for the treatment of cutaneous melanoma.

Indexed as

Disease ProgressionCell Cycle ProteinsCell Line, TumorCell MovementCell ProliferationCutaneous Malignant MelanomaFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansMaleMelanomaMiddle AgedNeoplasm InvasivenessPrognosisrho-Associated KinasesCDCA8 protein, humanCell Cycle Proteinsrho-Associated Kinases

Identifiers

PMID30431060
PMCPMC6257860
OpenAlexW2899806575

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.