甲状腺乳头状癌与喉鳞状细胞癌代谢组学初步研究

费梦嘉, 徐雅男, 王家东. 甲状腺乳头状癌与喉鳞状细胞癌代谢组学初步研究[J]. 临床耳鼻咽喉头颈外科杂志, 2017, 31(20): 1561-1565. doi: 10.13201/j.issn.1001-1781.2017.20.005
引用本文: 费梦嘉, 徐雅男, 王家东. 甲状腺乳头状癌与喉鳞状细胞癌代谢组学初步研究[J]. 临床耳鼻咽喉头颈外科杂志, 2017, 31(20): 1561-1565. doi: 10.13201/j.issn.1001-1781.2017.20.005
FEI Mengjia, XU Yanan, WANG Jiadong. Preliminary findings for metabolite profiles of papillary thyroid carcinoma and laryngeal squamous cell carcinoma[J]. J Clin Otorhinolaryngol Head Neck Surg, 2017, 31(20): 1561-1565. doi: 10.13201/j.issn.1001-1781.2017.20.005
Citation: FEI Mengjia, XU Yanan, WANG Jiadong. Preliminary findings for metabolite profiles of papillary thyroid carcinoma and laryngeal squamous cell carcinoma[J]. J Clin Otorhinolaryngol Head Neck Surg, 2017, 31(20): 1561-1565. doi: 10.13201/j.issn.1001-1781.2017.20.005

甲状腺乳头状癌与喉鳞状细胞癌代谢组学初步研究

  • 基金项目:

    上海高校选拔培养优秀青年教师科研专项基金 (No:101005.001.14.115)

详细信息
    通讯作者: 王家东, E-mail:drjiadongw@aliyun.com
  • 中图分类号: R736.1

Preliminary findings for metabolite profiles of papillary thyroid carcinoma and laryngeal squamous cell carcinoma

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  • 目的: 阐明甲状腺乳头状癌(PTC)与喉鳞状细胞癌(LSCC)的代谢组学特征并探讨其异同点。方法: 联合应用气相色谱-飞行时间质谱和超高效液相色谱-飞行时间质谱技术,对57例PTC和33例LSCC患者的新鲜肿瘤组织及其邻近非肿瘤组织的代谢物进行检测,获取代谢谱。应用单维、多维统计学方法分析肿瘤组织与邻近非肿瘤组织之间的差异代谢产物以及相关的代谢通路。结果: PTC以及LSCC患者肿瘤组织与邻近非肿瘤组织分别存在46及41种差异代谢产物。两组患者共同的代谢特征主要表现在肿瘤组织中糖酵解、氨基酸代谢、一碳代谢及色氨酸代谢均较邻近非肿瘤组织明显增强。PTC与LSCC肿瘤组织中的嘌呤和嘧啶代谢产物较邻近非肿瘤组织增多,牛磺酸和次牛磺酸的代谢产物在PTC肿瘤组织中增多。脂肪酸代谢产物在PTC以及LSCC中又呈现共性的降低。结论: PTC与LSCC既具有肿瘤组织中糖酵解、氨基酸代谢、一碳代谢及色氨酸代谢明显增强的共性代谢特点,又具有各自独特的代谢特征,这些特征的揭示有助于阐明上述肿瘤的生物学特征。
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  • [1]

    SIEGEL R L, MILLER K D, JEMAL A.Cancer statistics, 2016[J].CA Cancer J Clin, 2016, 66:7-30.

    [2]

    REINERS C, WEGSCHEIDER K, SCHICHA H, et al.Prevalence of thyroid disorders in the working population of Germany:ultrasonography screening in 96, 278unselected employees[J].Thyroid, 2004, 14:926-932.

    [3]

    BRITO J P, YARUR A J, PROKOP L J, et al.Prevalence of thyroid cancer in multinodular goiter versus single nodule:a systematic review and meta-analysis[J].Thyroid, 2013, 23:449-455.

    [4]

    HARACH H R, FRANSSILA K O, WASENIUS V M.Occult papillary carcinoma of the thyroid.A"normal"finding in Finland.A systematic autopsy study[J].Cancer, 1985, 56:531-538.

    [5]

    CONZO G, AVENIA N, BELLASTELLA G, et al.The role of surgery in the current management of differentiated thyroid cancer[J].Endocrine, 2014, 47:380-388.

    [6]

    QIU Y, CAI G, ZHOU B, et al.A distinct metabolic signature of human colorectal cancer with prognostic potential[J].Clin Cancer Res, 2014, 20:2136-2146.

    [7]

    DEJA S, DAWISKIBA T, BALCERZAK W, et al.Follicular adenomas exhibit a unique metabolic profile.1 H NMR studies of thyroid lesions[J].PLoS One, 2013, 8:e84637.

    [8]

    YAO Z, YIN P, SU D, et al.Serum metabolic profiling and features of papillary thyroid carcinoma and nodular goiter[J].Mol Biosyst, 2011, 7:2608-2614.

    [9]

    TRIPATHI P, KAMARAJAN P, SOMASHEKAR B S, et al.Delineating metabolic signatures of head and neck squamous cell carcinoma:phospholipase A2, apotential therapeutic target[J].Int J Biochem Cell B, 2012, 44:1852-1861.

    [10]

    SOMASHEKAR B S, KAMARAJAN P, DANCIU T, et al.Magic angle spinning NMR-based metabolic profiling of head and neck squamous cell carcinoma tissues[J].J Proteome Res, 2011, 10:5232-5241.

    [11]

    ERICKSON J W, CERIONE R A.Glutaminase:a hot spot for regulation of cancer cell metabolism[J]?Oncotarget, 2010, 1:734-740.

    [12]

    GATENBY R A, GILLIES R J.Why do cancers have high aerobic glycolysis[J]?Nat Rev Cancer, 2004, 4:891-899.

    [13]

    HU S, WANG J, JI E H, et al.Targeted Metabolomic Analysis of Head and Neck Cancer Cells Using High Performance Ion Chromatography Coupled with a Q Exactive HF Mass Spectrometer[J].Anal Chem, 2015, 87:6371-6379.

    [14]

    GAMCSIK M P, KASIBHATLA M S, TEETER S D, et al.Glutathione levels in human tumors[J].Biomarkers, 2012, 17:671-691.

    [15]

    LIU W, LE A, HANCOCK C, et al.Reprogramming of proline and glutamine metabolism contributes to the proliferative and metabolic responses regulated by oncogenic transcription factor c-MYC[J].Proc Natl Acad Sci U S A, 2012, 109:8983-8988.

    [16]

    DE INGENIIS J, RATNIKOV B, RICHARDSON A D, et al.Functional specialization in proline biosynthesis of melanoma[J].PLoS One, 2012, 7:e45190.

    [17]

    NILSSON R, JAIN M, MADHUSUDHAN N, et al.Metabolic enzyme expression highlights a key role for MTHFD2 and the mitochondrial folate pathway in cancer[J].Nat Commun, 2014, 5:e3128.

    [18]

    SON J, LYSSIOTIS C A, YING H, et al.Glutamine supports pancreatic cancer growth through a KRASregulated metabolic pathway[J].Nature, 2013, 496:101-105.

    [19]

    WEINBERG F, HAMANAKA R, WHEATON W W, et al.Mitochondrial metabolism and ROS generation are essential for Kras-mediated tumorigenicity[J].Proc Natl Acad Sci U S A, 2010, 107:8788-8793.

    [20]

    HOLM E, HAGMULLER E, STAEDT U, et al.Substrate balances across colonic carcinomas in humans[J].Cancer Res, 1995, 55:1373-1378.

    [21]

    ZHAI L, SPRANGER S, BINDER D C, et al.Molecular Pathways:Targeting IDO1 and Other Tryptophan Dioxygenases for Cancer Immunotherapy[J].Clin Cancer Res, 2015, 21:5427-5433.

    [22]

    ZAMANAKOU M, GERMENIS A E, KARANIKAS V.Tumor immune escape mediated by indoleamine 2, 3-dioxygenase[J].Immunol Lett, 2007, 111:69-75.

    [23]

    OPITZ C A, LITZENBURGER U M, SAHM F, et al.An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor[J].Nature, 2011, 478:197-203.

    [24]

    MORETTI S, MENICALI E, VOCE P, et al.Indoleamine2, 3-dioxygenase 1 (IDO1) is up-regulated in thyroid carcinoma and drives the development of an immunosuppressant tumor microenvironment[J].J Clin Endocr Metab, 2014, 99:e832-840.

    [25]

    SHIN J M, KAMARAJAN P, FENNO J C, et al.Metabolomics of Head and Neck Cancer:A Mini-Review[J].Front Physiol, 2016, 7:e26.

    [26]

    BATHEN T F, JENSEN L R, SITTER B, et al.MRdetermined metabolic phenotype of breast cancer in prediction of lymphatic spread, grade, and hormone status[J].Breast Cancer Res, 2007, 104:181-189.

    [27]

    TESSEM M B, SELNAES K M, SJURSEN W, et al.Discrimination of patients with microsatellite instability colon cancer using 1H HR MAS MR spectroscopy and chemometric analysis[J].J Proteome Res, 2010, 9:3664-3670.

    [28]

    EL AGOUZA I M, EISSA S S, EL HOUSEINI M M, et al.Taurine:a novel tumor marker for enhanced detection of breast cancer among female patients[J].Angiogenesis, 2011, 14:321-330.

    [29]

    LIN J, MANSON J E, SELHUB J, et al.Plasma cysteinylglycine levels and breast cancer risk in women[J].Cancer Res, 2007, 67:11123-11127.

    [30]

    SADZUKA Y, MATSUURA M, SONOBE T.The effect of taurine, a novel biochemical modulator, on the antitumor activity of doxorubicin[J].Biol Pharm Bull, 2009, 32:1584-1587.

    [31]

    DAIGELER A, CHROMIK A M, GEISLER A, et al.Synergistic apoptotic effects of taurolidine and TRAIL on squamous carcinoma cells of the esophagus[J].Int J Oncol, 2008, 32:1205-1220.

    [32]

    XU Y, ZHENG X, QIU Y, et al.Distinct Metabolomic Profiles of Papillary Thyroid Carcinoma and Benign Thyroid Adenoma[J].J Proteome Res, 2015, 14:3315-3321.

    [33]

    KUHAJDA F P.Fatty-acid synthase and human cancer:new perspectives on its role in tumor biology[J].Nutrition, 2000, 16:202-208.

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收稿日期:  2017-08-03

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