TY - JOUR
T1 - Serum microRNA profile enables preoperative diagnosis of uterine leiomyosarcoma
AU - Yokoi, Akira
AU - Matsuzaki, Juntaro
AU - Yamamoto, Yusuke
AU - Tate, Keisei
AU - Yoneoka, Yutaka
AU - Shimizu, Hanako
AU - Uehara, Takashi
AU - Ishikawa, Mitsuya
AU - Takizawa, Satoko
AU - Aoki, Yoshiaki
AU - Kato, Ken
AU - Kato, Tomoyasu
AU - Ochiya, Takahiro
N1 - Funding Information:
The authors thank Tomomi Fukuda, Takumi Sonoda, Hiroko Tadokoro, Megumi Miyagi and Tatsuya Suzuki for performing microarray assays, Junpei Kawauchi, Makiko Ichikawa and Satoshi Kondou, for technical support, Noriko Abe and Hiromi Sakamoto for the management of serum samples, Michiko Ohori for the management of personal information, and Hitoshi Fujimiya for developing in‐house analytic tools. Samples used in this study were obtained from the National Cancer Center Biobank, which is supported by the National Cancer Center Research and Development Fund (29‐A‐1). This study was financially supported through a “Development of Diagnostic Technology for Detection of miRNA in Body Fluids” grant from the Japan Agency for Medical Research and Development (to TO, 18ae0101011h0005).
Funding Information:
The authors thank Tomomi Fukuda, Takumi Sonoda, Hiroko Tadokoro, Megumi Miyagi and Tatsuya Suzuki for performing microarray assays, Junpei Kawauchi, Makiko Ichikawa and Satoshi Kondou, for technical support, Noriko Abe and Hiromi Sakamoto for the management of serum samples, Michiko Ohori for the management of personal information, and Hitoshi Fujimiya for developing in-house analytic tools. Samples used in this study were obtained from the National Cancer Center Biobank, which is supported by the National Cancer Center Research and Development Fund (29-A-1). This study was financially supported through a ?Development of Diagnostic Technology for Detection of miRNA in Body Fluids? grant from the Japan Agency for Medical Research and Development (to TO, 18ae0101011h0005).
Publisher Copyright:
© 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Uterine leiomyosarcoma (ULMS) is the major subtype of uterine sarcoma (US) and contributes to uterine cancer deaths. Although preoperative diagnosis of US remains challenging, frequent application of laparoscopic surgery for benign uterine leiomyomas (ULM) requires precise exclusion of US. MicroRNAs are stably present in the bloodstream, and the application of circulating miRNAs as disease biomarkers has been recognized. In the present study, we aimed to identify diagnostic biomarkers for distinguishing US from ULM by focusing on circulating miRNAs. All serum samples were collected preoperatively between 2009 and 2017, and all cases were histopathologically diagnosed. Whole miRNA profiles were obtained using a miRNA microarray. By analyzing expression levels of the miRNAs, candidate miRNAs were selected based on diagnostic performance in discriminating US from ULM, and a diagnostic model was then constructed. A total of 90 serum samples were analyzed, and clustering analyses revealed that the profiles of ULMS were distinct from those of controls. Based on leave-one-out cross-validation, seven miRNAs were selected as biomarker candidates. Based on model construction, the optimal model consisted of two miRNAs (miR-1246 and miR-191-5p), with an area under the receiver operating characteristic curve (AUC) for identifying ULMS of 0.97 (95% confidence interval [CI], 0.91-1.00). In contrast, serum lactate dehydrogenase had an AUC of only 0.64 (95% CI, 0.34-0.94). Seven serum miRNAs with high diagnostic performance for preoperative US screening were detected, and a promising diagnostic model for ULMS was generated.
AB - Uterine leiomyosarcoma (ULMS) is the major subtype of uterine sarcoma (US) and contributes to uterine cancer deaths. Although preoperative diagnosis of US remains challenging, frequent application of laparoscopic surgery for benign uterine leiomyomas (ULM) requires precise exclusion of US. MicroRNAs are stably present in the bloodstream, and the application of circulating miRNAs as disease biomarkers has been recognized. In the present study, we aimed to identify diagnostic biomarkers for distinguishing US from ULM by focusing on circulating miRNAs. All serum samples were collected preoperatively between 2009 and 2017, and all cases were histopathologically diagnosed. Whole miRNA profiles were obtained using a miRNA microarray. By analyzing expression levels of the miRNAs, candidate miRNAs were selected based on diagnostic performance in discriminating US from ULM, and a diagnostic model was then constructed. A total of 90 serum samples were analyzed, and clustering analyses revealed that the profiles of ULMS were distinct from those of controls. Based on leave-one-out cross-validation, seven miRNAs were selected as biomarker candidates. Based on model construction, the optimal model consisted of two miRNAs (miR-1246 and miR-191-5p), with an area under the receiver operating characteristic curve (AUC) for identifying ULMS of 0.97 (95% confidence interval [CI], 0.91-1.00). In contrast, serum lactate dehydrogenase had an AUC of only 0.64 (95% CI, 0.34-0.94). Seven serum miRNAs with high diagnostic performance for preoperative US screening were detected, and a promising diagnostic model for ULMS was generated.
KW - circulating microRNA
KW - diagnostic biomarkers
KW - liquid biopsy
KW - uterine leiomyosarcoma
KW - uterine sarcoma
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U2 - 10.1111/cas.14215
DO - 10.1111/cas.14215
M3 - Article
C2 - 31599471
AN - SCOPUS:85075211446
SN - 1347-9032
VL - 110
SP - 3718
EP - 3726
JO - Cancer Science
JF - Cancer Science
IS - 12
ER -