Alterations in patient plasma microRNA expression profiles following resection of metastatic melanoma

被引:29
作者
Latchana, Nicholas [1 ]
DiVincenzo, Mallory J. [2 ]
Regan, Kelly [3 ,4 ,5 ]
Abrams, Zachary [5 ]
Zhang, Xiaoli [5 ]
Jacob, Naduparambil K. [6 ]
Gru, Alejandro A. [7 ]
Fadda, Paolo [8 ,9 ]
Markowitz, Joseph [10 ]
Howard, J. Harrison [11 ]
Carson, William E., III [11 ]
机构
[1] Univ Toronto, Dept Gen Surg, Toronto, ON, Canada
[2] Ohio State Univ, Dept Vet Biosci, Columbus, OH 43210 USA
[3] Ohio State Univ, Med Scientist Training Program, Columbus, OH 43210 USA
[4] Ohio State Univ, Biomed Sci Grad Program, Columbus, OH 43210 USA
[5] Ohio State Univ, Dept Biomed Informat, Columbus, OH 43210 USA
[6] Ohio State Univ, Dept Radiat Oncol, Columbus, OH 43210 USA
[7] Univ Virginia, Dept Pathol, Charlottesville, VA 22903 USA
[8] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Arthur G James Comprehens Canc Ctr, Columbus, OH 43210 USA
[9] Ohio State Univ, Richard J Solove Res Inst, Columbus, OH 43210 USA
[10] H Lee Moffitt Canc Ctr & Res Inst, Dept Cutaneous Oncol, Tampa, FL USA
[11] Ohio State Univ, Dept Surg, Columbus, OH 43210 USA
关键词
miR; miR-1260a; miR-150-5p; miRNA; NanoString; CUTANEOUS MALIGNANT-MELANOMA; CANCER; DYSREGULATION; RECURRENCE; BIOMARKER; MIR-150; MIR-21; MIRNAS;
D O I
10.1002/jso.25163
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and ObjectivesMicroRNAs (miRs) are noncoding RNAs that regulate protein translation and melanoma progression. Changes in plasma miR expression following surgical resection of metastatic melanoma are under-investigated. We hypothesize differences in miR expression exist following complete surgical resection of metastatic melanoma. MethodsBlood collection pre- and post-surgical resection was performed in six individuals with solitary melanoma metastases. miR expression in extracted RNA was quantified using the NanoString nCounter Digital Analyzer. ResultsPre- and post-surgical plasma samples contained 216 miRs with expression above baseline. Comparison of postsurgical to preresection samples revealed differential expression of 25 miRs: miR-let-7a, miR-let7g, miR-15a, miR-16, miR-22, miR-30b, miR-126, miR-140, miR-145, miR-148a, miR-150-5p, miR-191, miR-378i, miR-449c, miR-494, miR-513b, miR-548aa, miR-571, miR-587, miR-891b, miR-1260a, miR 1268a, miR-1976, miR-4268, miR-4454 (P<0.05). Utilizing P<0.0046 as a cutoff to control for one false positive among the 216 miRs revealed that postsurgical melanoma plasma samples had upregulation of miR-1260a (P=0.0007) and downregulation of miR-150-5p (P=0.0026) relative to pre-surgical samples. ConclusionsDifferential expression of miR-150-5p and miR-1260a is present in plasma following surgical resection of metastatic melanoma in this small sample (n=6) of melanoma patients. Therefore, further investigation of these plasma miRs as noninvasive biomarkers for melanoma is warranted.
引用
收藏
页码:501 / 509
页数:9
相关论文
共 39 条
[1]   Dysregulation of miR-31 and miR-21 induced by zinc deficiency promotes esophageal cancer [J].
Alder, Hansjuerg ;
Taccioli, Cristian ;
Chen, Hongping ;
Jiang, Yubao ;
Smalley, Karl J. ;
Fadda, Paolo ;
Ozer, Hatice G. ;
Huebner, Kay ;
Farber, John L. ;
Croce, Carlo M. ;
Fong, Louise Y. Y. .
CARCINOGENESIS, 2012, 33 (09) :1736-1744
[2]   Identification of a Circulating MicroRNA Profile as a Biomarker of Metastatic Cutaneous Melanoma [J].
Armand-Labit, Virginie ;
Meyer, Nicolas ;
Casanova, Anne ;
Bonnabau, Henri ;
Platzer, Valerie ;
Tournier, Emilie ;
Sansas, Benoit ;
Verdun, Stephane ;
Thouvenot, Benoit ;
Hilselberger, Benoit ;
Doncescu, Andrei ;
Lamant, Laurence ;
Lacroix-Triki, Magali ;
Favre, Gilles ;
Pradines, Anne .
ACTA DERMATO-VENEREOLOGICA, 2016, 96 (01) :29-34
[3]   Comparisons of microRNA Patterns in Plasma before and after Tumor Removal Reveal New Biomarkers of Lung Squamous Cell Carcinoma [J].
Aushev, Vasily N. ;
Zborovskaya, Irina B. ;
Laktionov, Konstantin K. ;
Girard, Nicolas ;
Cros, Marie-Pierre ;
Herceg, Zdenko ;
Krutovskikh, Vladimir .
PLOS ONE, 2013, 8 (10)
[4]   NanoStriDE: Normalization and Differential Expression Analysis of NanoString nCounter Data [J].
Brumbaugh, Christopher D. ;
Kim, Hyunsung J. ;
Giovacchini, Mario ;
Pourmand, Nader .
BMC BIOINFORMATICS, 2011, 12
[5]   miRTarBase update 2018: a resource for experimentally validated microRNA-target interactions [J].
Chou, Chih-Hung ;
Shrestha, Sirjana ;
Yang, Chi-Dung ;
Chang, Nai-Wen ;
Lin, Yu-Ling ;
Liao, Kuang-Wen ;
Huang, Wei-Chi ;
Sun, Ting-Hsuan ;
Tu, Siang-Jyun ;
Lee, Wei-Hsiang ;
Chiew, Men-Yee ;
Tai, Chun-San ;
Wei, Ting-Yen ;
Tsai, Tzi-Ren ;
Huang, Hsin-Tzu ;
Wang, Chung-Yu ;
Wu, Hsin-Yi ;
Ho, Shu-Yi ;
Chen, Pin-Rong ;
Chuang, Cheng-Hsun ;
Hsieh, Pei-Jung ;
Wu, Yi-Shin ;
Chen, Wen-Liang ;
Li, Meng-Ju ;
Wu, Yu-Chun ;
Huang, Xin-Yi ;
Ng, Fung Ling ;
Buddhakosai, Waradee ;
Huang, Pei-Chun ;
Lan, Kuan-Chun ;
Huang, Chia-Yen ;
Weng, Shun-Long ;
Cheng, Yeong-Nan ;
Liang, Chao ;
Hsu, Wen-Lian ;
Huang, Hsien-Da .
NUCLEIC ACIDS RESEARCH, 2018, 46 (D1) :D296-D302
[6]   In-Silico Algorithms for the Screening of Possible microRNA Binding Sites and Their Interactions [J].
Dweep, Harsh ;
Sticht, Carsten ;
Gretz, Norbert .
CURRENT GENOMICS, 2013, 14 (02) :127-136
[7]   Identification of plasma microRNAs as new potential biomarkers with high diagnostic power in human cutaneous melanoma [J].
Fogli, Stefano ;
Polini, Beatrice ;
Carpi, Sara ;
Pardini, Barbara ;
Naccarati, Alessio ;
Dubbini, Nevio ;
Lanza, Maria ;
Breschi, Maria Cristina ;
Romanini, Antonella ;
Nieri, Paola .
TUMOR BIOLOGY, 2017, 39 (05)
[8]   Serum microRNAs as biomarkers for recurrence in melanoma [J].
Friedman, Erica B. ;
Shang, Shulian ;
de Miera, Eleazar Vega-Saenz ;
Fog, Jacob Ulrik ;
Teilum, Maria Wrang ;
Ma, Michelle W. ;
Berman, Russell S. ;
Shapiro, Richard L. ;
Pavlick, Anna C. ;
Hernando, Eva ;
Baker, Adam ;
Shao, Yongzhao ;
Osman, Iman .
JOURNAL OF TRANSLATIONAL MEDICINE, 2012, 10
[9]   Biomarker value and pitfalls of serum S100B in the follow-up of high-risk melanoma patients [J].
Gebhardt, Christoffer ;
Lichtenberger, Ramtin ;
Utikal, Jochen .
JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, 2016, 14 (02) :158-164
[10]   miR-21 and miR-155 are associated with mitotic activity and lesion depth of borderline melanocytic lesions [J].
Grignol, V. ;
Fairchild, E. T. ;
Zimmerer, J. M. ;
Lesinski, G. B. ;
Walker, M. J. ;
Magro, C. M. ;
Kacher, J. E. ;
Karpa, V. I. ;
Clark, J. ;
Nuovo, G. ;
Lehman, A. ;
Volinia, S. ;
Agnese, D. M. ;
Croce, C. M. ;
Carson, W. E., III .
BRITISH JOURNAL OF CANCER, 2011, 105 (07) :1023-1029