background image

匿堂壤连!Q塑生!魍筮!!鲞箜!嬲丛鲤垫坐曼!!嬲i垒丛坐:』坚呈Q嫂:!堂:!!:盟!:!

【7】

(8]

【9】

【10]

【11】

[12]

[13]

【14j

[15]

(16]

[17]

【lg】

囔静.辇凌众演蛋囊酶及葵捧麓秘与舞鬃臻转移瓣疆究遴疆

[jj.阖终医学如产科学分册,2005,32(1):54-56.

Herrera CA,Xu L,Bueana CD。et a1.Expression of

metastasis.re-

lated

genes

in

human epithelial

ovarian

tumors[J].ht

J Oncol,

2002,20(1):5—13.

Mitsiades N,Y#WH,Poulaki V。雒a1.Matrix metallopmteinase-7.
Mediated cleavage of

faslig

and

protect stumor

ceils from ehemo the

rapeutied

rugey

to

oxicity【J1.Cancer Res,2001,61(2):577-581.

Nishikawa A,1wasaki M,Akutagawa

N,et

a1.Expression of

various

matrix

proteases

and Ets family transcriptional factors

in

ovarian

cancer

celllines:correlation

to

invasive

potential【J】.Gynecol

On-

col,2000,79(2>:256_263.

Huang

S,VanArsdallM,Tedjarnti

S,eta/,Contributionsof stromal

metallopreteinase-9

to

angiogenesis

and growth of human

ovarian

carcinoma in

mice[J].J

Natl

Cancer

Inst,2002,94(15):

1134.1 142.

Lemy・Dudal J,Demeilliem C。G胡let O,et

a1.Transmigration

of hu—

mall

ovarian adenocareinoma

cells throllgh endothelialextraeellular

matrix

involves_v

integrins

and the

participation

of

MMP2[J】。轴

Cancer,2005

114(12):53l-543.

Murthi P,Barker G,Nowell CJ,et a1.PIasm inogen fragmentation
and increased production of extraeellularmatrix.degrading

protein.

age ale

associated

with

serous

epithelial

ovarian

progression[J】.

Gynecol Oncol,2004,92(1):80¥8。

Shigemasa K,Tanimoto H,Sakata K。越a1.Induction ofmatrix

met-

alloFotease-7

is common in mncinous

ovarian

tumors

including early

stage

diserse[J].Med

Oncol,2000。17(1):52-61.

Sakata K,Shigemasa K,Nagai N,et a1.Expression ofmatrix metal.

10proteinases(MMP2。MMp9.MTl一^藿MP)and

their inhibitors

《TIMPl,TIMP2)in

common epithelialtumors

oftheovary[j】.hat

Oncol,2000,17(4):673-681.

Murphy PM.Chemokines and the molecular basis 0f

cancer

metas-

tasis[J].N

Engl J

Med,2001,345(11):833-835.

蔡威,宋今丹.撼质金属蛋白酶及其组织抑制物在卵巢肿瘤巾

鹣表达f J],筑疰,2002,21(1):91-94.

Kim TJ。嚣聂o SB。Choi YL.篚a1.High

expression

oftissue inhibitor

of metalloproteinase-2

in

serous

ovarian

carcinomas

and

the role of

this

expression

in

ovarian tumorigenesis[J].Hum

Pathol,2006,37

(7):906.913.

【19】

[203

[21】

[22】

[23]

【24】

[25]

【26]

[27】

[28]

【嚣】

-65・

Fumya M,1.,shikura H,Kawarada Y,et

a/。Expression

of

matrix

metallopFoteinases

and。related

tissue

inhibitors

in

the

cyst

fluids of

ovariart mucinous

neoplasnls[J].Gynecol Oncol,2000,78(2):

106.1 12.

Demeter A,Szlrmai K。OIah

J,甜a/Elevated

expression of

matrix

metalloptroteinase-9and

flbronectin

concentration in

recurrent

epi.

thelial

Ovarian

cancer[J】。Orv

Hetil,2004,145(31):1617・1624,

Thorgeirsson

UP,Yoshiji

H,Sinha CC,et a1.Breast

cancer,tumor

noavascalature and the effect

of tissue

inhibitor

of

metalloproteinas.

e¥-l(TMP-1)on

Angiogenesis[J].In

Vivo,1996,10(2):

137.140.

Kim l,Kim HG。Moon SO。et

a1.Angiopoietin.1

induces endothelial

cellSpmuting through the activationof focal

adhe.sion

kinase and

plasmin

secretion(J].Circ Res,2000,86(9):952母59.

Patterson BC,Sang

QXA.Angiostatin—converting

enzyme

activities

of Human Matrily

sin(MMP-7)and

gelatinase

B/type

1V

collage-

nase(MMP-9)[J】.J

Biol

Chem,1997,272(46):28823-28825.

Hantke

B,Harbeck

N,Sehmalfeldt

B,et

a1.Clinical relevance of

matrix

metatloproteinase.13 determined with

new

highly

specific

and

sensitive

ELISA in

ascitic

fluid of

advanced

ovarian

carcinoma

patients【JJ.Biol Chem,2003,384(8):1247—1251.

胡晓霞,李力,黎捋戎,等.基质金属蛋白酶MMP母及其组织抑

铡测TlMP—l在郛黎瓣癯中的表达及意义[J】,孛潮妇产辩牾

凑杂盍,2004,5(2);123.1赞,
Wu

X,Li

H,Kang

L,et a1.Activated

matrix

metalloproteinase-2.

apotential marker of

prognosis

for epithelial

ovarian

cancer[J].Gy-

necol Oncol,2002.84(8):126一134.

Tomg

PL。Man

TL.Chan WY.雕a1.Prognostic significance of stre-

mal metalloproteinase-2

in ov矗rian

adenocarcinoma and

its

relation

to

carcinoma

progression【j j.Gynecol

Oncol,2004,92(4》:

559-567.

Kamat AA,FIetcher M.Gruman LM,et a1.The clinical rele2va

nce

of

st

romal

mat

rixmetallop roteinase

exp

i_ession

in

ovarla

nca ncer

【J1.Clin

Cancer

Res,2006,12(6):1707.1714.

Lakka

SS,Raian

M,Condi

C+et

a1.Adenovirus-mediated

a曜黔

sion of

antisense

MMP-9

in

glioma

cells inhibits

tumor

growth and

invasion【Jj.Oncogene,2002。21(5):801

1-8019.

收稿日期:2008-07-09修回日期:2008.10-15

维生素D及其受体在妇科肿瘤中的研究进展

兰A(综述),郑

秀(审校)

<禳建叛辩大学瓣鬟繁一医菝羟产辩,鼷髑350005)

中圈分类号:R737.3

文献标识鹤:A

文黛编号:1006-2084(2009)01-0065-04

擒要:维生囊D受体(VDR)楚奔导l,25二疑维生素B3发撂嶷转效应的核农生物大分子,菇类

瓣薛激素/甲获撩受落起家族残燕。l,25二羟缍燕素D3是橥垒褰转鳇活整形武,它除了英凑钙、磷

代谢调节作用井,还能调节正常组织和肿瘤细胞的生长和分化。VDR基因上存农多个多态性戗点,

鸯部分肿瘤的发生发展密切相关。本文主要综述VDR的结构及熊功能、基因多态性,维生素D的细

胞作用机制及与妇科肿瘤的相关性研究。

荚键谲:维童豢D;维生素D受露;据翳脖瘰

Research Advances of Vitamin D

and

Its Receptor in Gynecologic Tumor 班N/an.ZHENG Xiu.(De-

partment

of

Obstetrics&Gynecology,the

First

A.融ed

Hospital

of Fufian

Medical University.Fudwu

350005.China)

Abstract:弧e

vitumin

receptor(VDR)is

intranuclear

Biological㈣remoleeules.The

biologieal

ae.

tions of l,25・Dihydroxyvitamin D3 a辩primarily mediated by the VDR,which belongs

to the

superfamily of

steriod/thyroid hormone nuclear

receptors.强e

vitamin

D,l,25.Dihydroxyvitamin

D,is

the

active

metabolite

of vitamin

D,aoart

from

tlle

metabolic regulation of calcium

and

phosphate。it has

normal

regulation

and

tUmor

eell growth and differentiation+The

VDR gene

exists several polymorphisms。which is closely related

to

part

of

the tumor

ocettrrence

and

development.This

article

reviewed

the

structure,function

and

genetic

poly.

morphisms of VDR

gene,and

the cellular mechanism

of vitamin D in

gynecologic

oncdogy。

Key words:Vitamin

D;Vitamin

D receptor:Gynecologic tumor

透年来,亿疗在治疗多

数妇科恶性肿瘤孛发挥越来

越重要的作用,但是,化疗药

物存在较严重的毒性和耐药

性,限制了其在临床上的应

用。维生素D是人体必需

的维生索,除了调节体内钙、

磷代谢之外,还具有诱导细

臆分化、搀剜细胞增殖、促进

肿瘤细胞凋亡以及免疫调节

作用。在卵巢癌、子宫内膜

癌及宫颈癌中已检测到维生

素p受体(vitamin

D recep-

万方数据