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宫颈鳞状细胞癌化疗前后Bcl-2、VEGF变化与疗效的关系 被引量:1

Relationship between the changes of Bel-2 and VEGF and the therapeutic effects before and after SIP chemotherapy for cervical squamous cell carcinoma
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摘要 目的探讨奈得铂(S)、异环磷酰胺(I)、硫酸培洛霉素(P)并用(SIP疗法)化疗与宫颈鳞状细胞癌组织中Bcl-2、VEGF变化的关系。方法以2000年1月至2002年9月日本北里大学病院妇产科收治的48例宫颈鳞状细胞癌患者为研究对象,采用SIP疗法治疗1~2个疗程,MRI判断疗效;采用免疫组化法检测有效组与无效组化疗前后组织标本中Bcl-2、VEGF阳性表达率。结果有效组化疗前后Bcl-2阳性表达率分别为67%(19/28)和35%(10/28),差异有统计学意义(χ2=5.7931,P<0.05)。无效组化疗前后阳性表达率分别为30%(6/20)、40%(8/20),差异无统计学意义(χ2=0.4396,P>0.05);有效组在化疗前Bcl-2阳性表达率为67%,明显高于无效组30%(χ2=6.6997,P<0.05)。有效组化疗前后VEGF阳性表达率分别为89%(25/28)和42%(12/28),差异有统计学意义(χ2=13.4623,P<0.05)。无效组化疗前后VEGF阳性表达率差异无统计学意义(χ2=2.8490,P>0.05)。有效组在化疗前VEGF阳性表达率(89%)明显高于无效组(55%)(χ2=7.3143,P<0.05)。结论化疗前高表达的Bcl-2、VEGF预示着宫颈鳞状细胞癌采用SIP化疗有效;1疗程结束后组织标本中Bcl-2、VEGF的快速降低对是否需要继续进行多疗程化疗有提示作用。 Objective To determine whether or not Bcl-2 and VEGF obtained from biopsy specimens were useful as predictors of NAC response. Methods Totally 48 cases of cervical carcinoma were treated with 1 to 2 courses of SIP therapy. The response to SIP was measured by magnetic resonance imaging(MRI). The biopsy specimens from 48 patients with cervical carcinoma before and after SIP therapy were evaluated for Bcl-2 and VEGF proteins expressions by LSAB immunohistochemistry. Results In chemotherapy-effective patients, the expression rates of Bcl-2 protein before and after chemotherapy were 67% (19/28 )and 35 % (10/28), respectively (χ^2 = 5. 7931, P 〈 0. 05 ) ; in non-chemotherapy effective patients,the expression rates of Bcl-2 protein before and after chemotherapy were 30% (6/20) and 40% (8/20), respectively(χ^2 =0. 4396,P 〉0. 05) ; in chemotherapy effective patients,the expression rates of VEGF protein before and after chemotherapy were 89% (25/28) and 42% ( 12/28), respectively( χ^2 = 13. 4623, P 〈 0. 05 ) ; in chemotherapy noneffective patients,the expression rates of VEGF protein before and after chemotherapy were 55% (11/20)and 80% (16/ 20), respectively( χ^2 = 2. 8490,P 〉 0. 05 ). Conclusion NAC with Nedaplatin, ifosfamide and peplomycin is effective for patients with locally advanced squamous cell carcinoma of cervix. Alterations of Bcl-2 and VEGF can be predictors for NAC.
出处 《中国实用妇科与产科杂志》 CAS CSCD 北大核心 2009年第4期290-292,共3页 Chinese Journal of Practical Gynecology and Obstetrics
关键词 宫颈鳞状细胞癌 奈得铂 异环磷酰胺 硫酸培洛霉素 BCL-2 VEGF cervical carcinoma nedaplation ifosfamide peplomycin Bcl-2 VEGF
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  • 1平林光司 岗田悦子 中妻嘉夫 等.SIP治疗浸润、再发宫颈癌的临床研究.日本妇产科杂志,1992,44:341-348.
  • 2对木章 大谷贵美 铃木卓 等.宫颈癌术前硫酸培洛霉素,异环磷酰胺,奈得铂疗法.日本妇产科杂志,2002,54:633-637.
  • 3Hwang YY, Moon H , Cho SH , et al. Ten-year survival of patients with locally advanced stage Ⅰb2 and Ⅱb cervical cancer after neoadjuvant chemotherapy and radical hysterectomy [ J] . Gynecol Oncol , 2001 , 82 (4) :402-408.
  • 4Huang HJ , Chang TC , Hong JH , et al . Prognostic value of age and histologic type in neoadjuvant chemotherapy plus radical surgery for bulky ( ≥ 4 cm) stage Ⅰb and Ⅱa cervical carcinoma[J]. Int J Gynecol'Cancer , 2003 , 13 : 204-211.
  • 5Bolis G, van Zainten PI, Scarfone G, et al. Determinants of response to a cisplatin-based regimen as neoadjuvant chemotherapy in stage Ⅰb - Ⅱa invasive cervical cancer[ J] . Gynecol Oncol , 1996 , 63 : 62-65.
  • 6胡秀峰,周芳.血清TSP-1、VEGF对评价食管癌患者化疗疗效的意义[J].实用癌症杂志,2007,22(1):37-40. 被引量:5
  • 7高岩,彭芝兰.宫颈鳞癌及新辅助化疗对血清VEGF表达的影响[J].华西医学,2007,22(3):513-514. 被引量:2
  • 8Reed JC. Bcl-2 and the regulation of programmed cell death[ J]. J Cell Biol, 1993,75(2) :241-243.
  • 9李勇,潘立峰,赵群,刘冀红,范立桥,刘品一,马志学,于跃明.化疗药物诱导人胃癌细胞凋亡及Bcl-2、Bax基因蛋白表达变化的研究[J].河北医科大学学报,2001,22(3):163-165. 被引量:6

二级参考文献27

  • 1Hug H. Fas-mediated apoptosis intumor and defense. Biol Chem,1997,378(12): 1405
  • 2Ohmori T, Podack ER, Nishio K, et al. Apoptosis of lung cancer cells caused by someanti-cancer agents (MMC, CPT-11, and ADM) is inhibited by Bcl-2. Biochem Bioph Res Commun,1993,1921 (1): 30
  • 3Oltavai ZN,Millimen CL,Korsmeyer SJ,et al. Bcl-2 heterodimerizes in vivo withconserved homolog, Bax, that accelerates programmed cell death. Cell, 1993,74 (4): 609
  • 4Boise LH, Gonzalez-Garcia M, Postema CE, et al. Bcl-x, a Bcl-2 related gene thatfunctions as dominant regulator of apoptotic cell death. Cell, 1993,74 (3): 597
  • 5Yang E,Zha JP,Jockel J ,et al. Bad,a heterodimeric partner for BclXL and Bcl-2,displaces Bax and promotes cell death. Cell, 1995,80 (2):285
  • 6Takayama S, Sato T, Krajewski S, et al. Cloning and functional analysis of BAG-1: anovel Bcl-2 binding protein with anti-cell death activity. Cell, 1995,80 (2): 279
  • 7Reed JC. Bcl-2 and the regulation of programmed cell death. J Cell Bid, 1993,75(2):241
  • 8Miyashita T, Reed JC. Bcl-2 oncoprotein block cheotherapyinduced apoptosis in ahuman leukemia cell line. Blood, 1993,81 (1): 151
  • 9Vescio R,Berenson J. Lichtenstein aupregulated expression of Bcl-2inmutiplemyltiple myeloma cells induced by exposure to doxorubicin etoposideand hydrogenperoxide. Blood, 1996,88(5): 1805
  • 10Naumann U, Weller M. Retroviral Bax gene transfer fails to sensitize malignantglioma cell to CD95L-induced apoptosis and cancer chemotherapy. Iht J Cancer, 1998,77(4):645

共引文献10

同被引文献9

  • 1魏玮,程玉峰,姜玉华,梁业民,乔乃安.Bax、Bcl-2ASODN联合转染增强宫颈癌HeLa细胞放射敏感性的实验研究[J].现代妇产科进展,2006,15(11):841-843. 被引量:9
  • 2Fabrini MG, Gadducci A, Perrone F, et al. Clinical outcome of tailored adjuvant postoperative chemoradiotherapy in IB FIGO stage cervical cancer[J]. Anticance Res, 2009,29 : 4205-4210.
  • 3Law CL, Gordon KA, Collier J, et al. Preclinical antilymphoma activity of a humanized anti-CD40 monoclonal anti-body, SGN-40 [ J ]. Cancer Res, 2005,65 : 8331-8338.
  • 4Zhou ZH, Wang JF, Wang YD, et al. An agonist anti-human CD40 monoclonal antibody that induces dendritic cell formation and maturation and inhibits proliferation of a myeloma cell line[ J]. Hybridoma, 1999,18:471-478.
  • 5Zhou ZH, Shi Q, Wang JF, et al. Sensitization of multiple myeloma and B lymphoma lines to dexamethasone and γ- radiation-induced apoptosis by CD40 activation[ J ]. Apoptosis ,2005,10 : 123-134.
  • 6Qu QX, Ge Y, Chen Y J, et al. Preparation and characterization of a novel chimeric antibody against human CD40 with the potential to inhibit daudi cell proliferation [ J ]. Hybridoma ,2009,28 : 121-128.
  • 7Groeger AM,Esposito V, De Luca A, et al. Prognostic value of immunohistochemical expression of p53, Bax, Bcl-2 and Bcl-xL in resected non-small cell lung cancers [ J]. Histopathology, 2004,44 : 54 -63.
  • 8Zhao DL, Shi JS,Li MZ, et al. The expression of apoptosis related genes bcl-2 and bax protein and apoptosis positivity in cervical carcinoma during irradiation[ J ]. J Clin Oncol ,2005,4 : 105-107.
  • 9Hernandez P, Olivera P, Duenas-Gonzalez A, et al. Gemcitabine activity in cancer cell lines [ J ]. Cancer Chemother Pharmacol,2001,48 :488-492.

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