磷脂酶参与的花生四烯酸12-LOX代谢通路在喉鳞状细胞癌中的作用及临床意义

王嘉, 李晓明, 徐鸥, 等. 磷脂酶参与的花生四烯酸12-LOX代谢通路在喉鳞状细胞癌中的作用及临床意义[J]. 临床耳鼻咽喉头颈外科杂志, 2013, 27(24): 1355-1359. doi: 10.13201/j.issn.1001-1781.2013.24.008
引用本文: 王嘉, 李晓明, 徐鸥, 等. 磷脂酶参与的花生四烯酸12-LOX代谢通路在喉鳞状细胞癌中的作用及临床意义[J]. 临床耳鼻咽喉头颈外科杂志, 2013, 27(24): 1355-1359. doi: 10.13201/j.issn.1001-1781.2013.24.008
WANG Jia, LI Xiaoming, XU Ou, et al. The role and clinical significance of 12-LOX passway in arachidonic acid metabolism induced by phospholipase Cγ-2 in laryngeal squamous cell carcinoma[J]. J Clin Otorhinolaryngol Head Neck Surg, 2013, 27(24): 1355-1359. doi: 10.13201/j.issn.1001-1781.2013.24.008
Citation: WANG Jia, LI Xiaoming, XU Ou, et al. The role and clinical significance of 12-LOX passway in arachidonic acid metabolism induced by phospholipase Cγ-2 in laryngeal squamous cell carcinoma[J]. J Clin Otorhinolaryngol Head Neck Surg, 2013, 27(24): 1355-1359. doi: 10.13201/j.issn.1001-1781.2013.24.008

磷脂酶参与的花生四烯酸12-LOX代谢通路在喉鳞状细胞癌中的作用及临床意义

详细信息
    通讯作者: 单春光,E-mail:shanchunguang@163.com
  • 中图分类号: R739.65

The role and clinical significance of 12-LOX passway in arachidonic acid metabolism induced by phospholipase Cγ-2 in laryngeal squamous cell carcinoma

More Information
  • 目的:研究磷脂酶(PL)Cγ-2、花生四烯酸(AA)以及脂加氧酶-12(12-LOX)在喉鳞状细胞癌中的表达情况,探讨脂质代谢与喉鳞状细胞癌的关系。方法:选取30例喉癌组织以及癌旁组织(均经病理检查为正常组织),以免疫组织化学法(SP法)检测PLCγ-2和12-LOX的表达,以气相色谱联合质谱法检测AA的含量。结果:喉癌组织中PLCγ-2和12-LOX的表达高于正常组织(P<0.05),而AA含量低于正常组织(P<0.05);PLCγ-2和12-LOX与喉癌的临床分期、病理分化以及淋巴结转移有密切关系(P<0.05);AA与喉癌的临床分期、病理分化以及淋巴结转移无关(P>0.05);PLCγ-2、AA以及12-LOX与年龄无关(P>0.05)。结论:PLCγ-2、AA和12-LOX三者与喉癌关系密切,阻断此通路,可能对喉癌的治疗有一定的意义。
  • 加载中
  • [1]

    宣卓琦, 丁永斌. AA代谢与肿瘤的研究进展[J]. 西部医学, 2009, 21(10):1809-1811.

    [2]

    HERMANOVA M, KARASEK P, TOMASEK J, et al. Comparative analysis of clini copathological correlations of cyclooxygenase-2 expression in resectable pancreatic cancer[J]. World J Gastroenterol, 2010, 16:1879-1884.

    [3]

    ZHANG B, WU Q, YE X F,et al. Roles of PLC-gamma2 and PKCalpha in TPA-induced apoptosis of gastric cancer cells[J]. World J Gastroenterol,2003,9:2413-2418.

    [4]

    KIM K M, KANG D W, MOON W S, et al. PKCtheta expression in gastrointestinal stromal tumor[J].Mod Pathol, 2006,19:1480-1486.

    [5]

    陈启, 白丽. 磷脂酶Cγ2与B淋巴细胞[J]. 国际免疫学杂志, 2009, 32(5):372-375.

    [6]

    WEBER M, TREANOR B, DEPOIL D, et al. Phospholipase C-gamma2 and Vav cooperate within signaling microclusters to propagate B cell spreading in response to membranebound antigen[J]. Exp Med, 2008, 205:853-868.

    [7]

    白洁, 罗深秋, 冀群升. 磷脂酶C-γ2对鼠成纤维细胞株迁移能力的影响[J]. 生命科学研究, 2001, 5(1):33-38.

    [8]

    CAMPOS A C, MOLOGNONI F, MELO F H, et al. Oxidative stress modulates DNA methylation during melanocyte anchorage blockade associated with malignant transformation[J]. Neoplasia, 2007, 9:1111-1121.

    [9]

    PEJIC S, KASAPOVIE J, TODOROVIC A, et al. Lipid peroxideation and antioxidant status in blood of patients with uterine myoma, endometrium[J]. Biol Res, 2006, 39:619-629.

    [10]

    PATEL B P, RAWAL U M, DAVE T K, et al. Lipid peroxideation total antioxidant status, and total thiol levels predict overall survival in patients with oral squamous cell carcinoma[J]. Integr Cancer Ther, 2007, 6:365-372.

    [11]

    TSAO S M, YIN M C, LIU W H, et al. Oxidant stress and B vitamins status in patients with nonsmall cell lung cancer[J]. Nutr Cancer, 2007,59:8-13.

    [12]

    FREEMAN E J, SHEAKLEY M L, CLEMENTS R J. Angiotensin II dependent growth of vascular smooth muscle cells requires transactivation of the epidermal growth factor receptor via a cytosolic phospholipase A(2)mediated release of arachidonic acid[J]. Arch Biochem, 2010, 498:50-56.

    [13]

    SCHÖNFELD P, WOJTCZAK L. Fatty acids decrease mitochondrial generation of reactive oxygen species at the reverse electron transport but increase it at the forward transport[J]. Biochim Biophys Acta,2007,1767:1032-1040.

    [14]

    KEANE D C, TAKAHASHI H K, DHAYAL S,et al. Arachidonic acid actions on functional integrity and attenuation of the negative effects of palmitic acid in a clonal pancreatic β-cell line[J]. Clin Sci(Lond),2011, 120:195-206.

    [15]

    PALOMBA L, CERIONI L, CANTONI O. Arachidonic acid inhibits neuronal nitric oxide synthase elicited by proinflammatory stimuli and promotes astrocyte survival with both exogenous and endogenous peroxynitrite via different mechanisms[J]. J Neurosci Res, 2010, 88:2459-2468.

    [16]

    MOHAMMAD A M, ABDEL H A, ABDEL W, et al. Expression of cyclooxyge nase-2 and 12-lipoxygenase in human breast cancer and their relationship with HER-2/neu and hormonal receptors:impact on prognosis and therapy[J]. Indian J Cancer, 2006,43:163-168.

    [17]

    BEDNAR W, HOLZMANN K, MARIAN B. Assessing 12(S)-lipoxygenase inhibit tory activity using colorectal cancer cells overexpressing the enzyme[J]. Food Chem Toxicol, 2007, 45:508-514.

    [18]

    NIE D, TANG K, SZEKERES K, et al. Eicosanoid regulation of angiogenesis in human prostate carcinoma and its therapeutic implications[J]. Ann N Y Acad Sci,2000, 905:165-176.

    [19]

    NIE D, KRISHNAMOORTHY S, JIN R, et al. Mechanisms regulating tumor angio genesis by 12-lipoxygenase in prostate cancer cells[J]. Biol Chem, 2006, 281:18601-18609.

    [20]

    WINER I, NORMOLLE D P, SHUREIQI I, et al. Expression of 12-lipoxygenase as a biomarker for melanoma carcinogenesis[J]. Melanoma Res, 2002, 12:429-434.

    [21]

    邓君健, 徐细明. 脂加氧酶在肿瘤中的研究进展[J]. 肿瘤学杂志,2011, 17(4):289-293.

    [22]

    KRISHNAMOORTHY S, JIN R, CAI Y, et al. 12-Lipoxygenase and the regulation of hypoxiainducible factor in prostatecancer cells[J]. Exp Cell Res, 2010, 316:1706-1715.

    [23]

    SUTCLIFFE S, PLATZ E A. Inflammation and prostate cancer:a focus on infections[J]. Curr Urol Rep, 2008,9:243-249.

    [24]

    MBEUNKUI F, JOHANNN D J. Cancer and the tumor microenvironment:a review of an essential relationship[J]. Cancer Chemother pharmacol, 2009, 63:571-582.

    [25]

    ZHANG X, NIE D, CHAKRABARTY S. Growth factors in tumor microenvironment[J]. Front Biosci(Landmark Ed),2010,15:151-165.

    [26]

    MALETZKI C, EMMRICH J. Inflammation and immunity in the tumor environment[J]. Dig Dis,2010,28:574-578.

    [27]

    DUAN R D, NILSSON A. Metabolism of sphingolipids in the gut and its relation to inflammation and cancer development[J]. Prog Lipid Res, 2009,48:62-72.

    [28]

    BANIYASH M. Chronic inflammation, immunosuppression and cancer. new insights and outlook[J]. Semin Cancer Biol, 2006, 16:80-88.

  • 加载中
计量
  • 文章访问数:  159
  • PDF下载数:  104
  • 施引文献:  0
出版历程
收稿日期:  2013-01-30

目录