Matches in SemOpenAlex for { <https://semopenalex.org/work/W2885281644> ?p ?o ?g. }
- W2885281644 endingPage "4768" @default.
- W2885281644 startingPage "4755" @default.
- W2885281644 abstract "An integrated bioinformatical analysis to evaluate the role of KIF4A as a prognostic biomarker for breast cancer Dan Xue,1,* Pu Cheng,2,* Mengjiao Han,3 Xiyong Liu,4,5 Lijun Xue,6 Chenyi Ye,7 Ke Wang,8 Jian Huang8,9 1Department of Plastic Surgery, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China; 2Department of Gynaecology, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China; 3Department of Medical Oncology, Key Laboratory of Biotherapy in Zhejiang, Sir Run Run Shaw Hospital, Medical School of Zhejiang University, Hangzhou, China; 4Biomarker Development, California Cancer Institute, Temple City, CA, USA; 5School of Medicine, Taipei Medical University, Taipei, Taiwan, Republic of China; 6Department of Pathology, Loma Linda University Medical Center, Loma Linda, CA, USA; 7Department of Orthopaedics, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China; 8Department of Surgical Oncology, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China; 9Gastroenterology Institute, Zhejiang University School of Medicine, Hangzhou, China *These authors contributed equally to this work Purpose: The aim of this study was to investigate the diagnostic and prognostic value of human kinesin family member 4A (KIF4A) as an effective biomarker for breast cancer.Materials and methods: Cancer Genome Atlas data and 12 independent public breast cancer microarray data sets were downloaded and analyzed using individual and pooled approaches.Results: The results of our study revealed a strong and positive correlation between KIF4A expression and malignant features of breast cancer. KIF4A had a strong prognostic value in both ER-positive and ER-negative breast cancers comparable to or even better than tumor size, lymph node invasion, and Elston grade. We also found that KIF4A might be the target gene of microRNA-335, which can suppress KIF4A expression by targeting the 3′-untranslated region of its mRNA.Conclusion: KIF4A might serve as a robust prognostic predictor for breast cancer. Targeting KIF4A activity could be a promising therapeutic option in breast cancer treatment. Keywords: breast cancer, KIF4A, microarray, microRNA, prognosis" @default.
- W2885281644 created "2018-08-22" @default.
- W2885281644 creator A5006120530 @default.
- W2885281644 creator A5012762146 @default.
- W2885281644 creator A5026906414 @default.
- W2885281644 creator A5031124433 @default.
- W2885281644 creator A5052469066 @default.
- W2885281644 creator A5064261255 @default.
- W2885281644 creator A5081487015 @default.
- W2885281644 creator A5085596965 @default.
- W2885281644 date "2018-08-01" @default.
- W2885281644 modified "2023-09-25" @default.
- W2885281644 title "An integrated bioinformatical analysis to evaluate the role of KIF4A as a prognostic biomarker for breast cancer" @default.
- W2885281644 cites W144423133 @default.
- W2885281644 cites W1536340771 @default.
- W2885281644 cites W1964368719 @default.
- W2885281644 cites W1965371218 @default.
- W2885281644 cites W1967369606 @default.
- W2885281644 cites W1972240813 @default.
- W2885281644 cites W1972324535 @default.
- W2885281644 cites W1972671582 @default.
- W2885281644 cites W1976173969 @default.
- W2885281644 cites W1987004461 @default.
- W2885281644 cites W1992887353 @default.
- W2885281644 cites W1996445359 @default.
- W2885281644 cites W2001469879 @default.
- W2885281644 cites W2001707140 @default.
- W2885281644 cites W2011192510 @default.
- W2885281644 cites W2012031864 @default.
- W2885281644 cites W2017570593 @default.
- W2885281644 cites W2017600542 @default.
- W2885281644 cites W2024544530 @default.
- W2885281644 cites W2044702943 @default.
- W2885281644 cites W2045765066 @default.
- W2885281644 cites W2045842462 @default.
- W2885281644 cites W2066655755 @default.
- W2885281644 cites W2068827505 @default.
- W2885281644 cites W2075165253 @default.
- W2885281644 cites W2097017184 @default.
- W2885281644 cites W2105133921 @default.
- W2885281644 cites W2106174403 @default.
- W2885281644 cites W2106259349 @default.
- W2885281644 cites W2110237047 @default.
- W2885281644 cites W2110993628 @default.
- W2885281644 cites W2116077607 @default.
- W2885281644 cites W2128985829 @default.
- W2885281644 cites W2130410032 @default.
- W2885281644 cites W2132523282 @default.
- W2885281644 cites W2132893003 @default.
- W2885281644 cites W2134197585 @default.
- W2885281644 cites W2137319707 @default.
- W2885281644 cites W2138752269 @default.
- W2885281644 cites W2142614171 @default.
- W2885281644 cites W2147908679 @default.
- W2885281644 cites W2150257204 @default.
- W2885281644 cites W2150671673 @default.
- W2885281644 cites W2153961241 @default.
- W2885281644 cites W2155098031 @default.
- W2885281644 cites W2156711378 @default.
- W2885281644 cites W2157840751 @default.
- W2885281644 cites W2158501247 @default.
- W2885281644 cites W2160450758 @default.
- W2885281644 cites W2160928966 @default.
- W2885281644 cites W2161770015 @default.
- W2885281644 cites W2163563958 @default.
- W2885281644 cites W2164194749 @default.
- W2885281644 cites W2169143409 @default.
- W2885281644 cites W2329659234 @default.
- W2885281644 cites W2331186405 @default.
- W2885281644 cites W2416227107 @default.
- W2885281644 cites W2427820952 @default.
- W2885281644 cites W2570618306 @default.
- W2885281644 cites W2578010562 @default.
- W2885281644 cites W2584989749 @default.
- W2885281644 cites W2597941589 @default.
- W2885281644 cites W2615012088 @default.
- W2885281644 cites W2626167111 @default.
- W2885281644 cites W2723579800 @default.
- W2885281644 cites W2725351446 @default.
- W2885281644 cites W2734616814 @default.
- W2885281644 cites W2743377907 @default.
- W2885281644 cites W2751197790 @default.
- W2885281644 cites W2915478882 @default.
- W2885281644 doi "https://doi.org/10.2147/ott.s164730" @default.
- W2885281644 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6091482" @default.
- W2885281644 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30127624" @default.
- W2885281644 hasPublicationYear "2018" @default.
- W2885281644 type Work @default.
- W2885281644 sameAs 2885281644 @default.
- W2885281644 citedByCount "15" @default.
- W2885281644 countsByYear W28852816442019 @default.
- W2885281644 countsByYear W28852816442020 @default.
- W2885281644 countsByYear W28852816442021 @default.
- W2885281644 countsByYear W28852816442022 @default.
- W2885281644 countsByYear W28852816442023 @default.
- W2885281644 crossrefType "journal-article" @default.
- W2885281644 hasAuthorship W2885281644A5006120530 @default.
- W2885281644 hasAuthorship W2885281644A5012762146 @default.