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层粘连蛋白受体1在部分性和完全性葡萄胎蜕膜细胞上的过表达。

Overexpression of laminin receptor 1 on decidual cells in partial and complete mole.

作者信息

Nagymanyoki Zoltan, Callahan Michael J, Parast Mana M, Berkowitz Ross S, Mok Samuel C, Fulop Vilmos

机构信息

Division of Gynecologic Oncology, New England Trophoblastic Disease Center, Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

出版信息

Gynecol Oncol. 2008 Jan;108(1):121-5. doi: 10.1016/j.ygyno.2007.08.097. Epub 2007 Oct 24.

Abstract

OBJECTIVES

Laminin receptor 1 (LR1), a non-integrin-type laminin receptor, has been described in several tumors and may play a role in tumor invasion. It is well known that LR1 can modify the conformation and degradation of laminin thus enhancing tumor cell invasion. LR1 may play a role in controlling trophoblast invasion in normal and molar pregnancies.

MATERIALS AND METHODS

Real-time polymerase chain reaction (RT-PCR) was performed on total cDNA from 17 gestational age-controlled normal placentas, 10 complete moles (CM), and 4 partial moles (PM). Immunolocalization of LR1 was performed on paraffin sections prepared from 17 age-controlled placentas, 17 PM, and 19 CM.

RESULTS

RT-PCR demonstrated a 13-fold increase in LR1 mRNA expression in molar tissues (PM and CM combined) versus normal placentas (p=0.012). Immunohistochemical analysis revealed LR1 localized to the decidual cells. In normal placenta LR1 localized to the decidual cell membrane. However, in PM and CM, LR1 was additionally noted in the cytoplasm of decidual cells. Interestingly, with immunohistochemistry method, we found that PM demonstrated higher protein expression of LR1 than either normal placenta or CM (p=0.001 and p=0.024, respectively).

CONCLUSION

LR1 is expressed in both the decidual cells of normal placenta and mole (CM and PM). Decidual cells in CM and PM express LR1 significantly greater than the decidual cells in placenta. The underlying mechanism of how molar tissue may be associated with enhanced expression of LR1 in the maternal endometrium is unclear.

摘要

目的

层粘连蛋白受体1(LR1)是一种非整合素型层粘连蛋白受体,已在多种肿瘤中被描述,可能在肿瘤侵袭中发挥作用。众所周知,LR1可改变层粘连蛋白的构象并促进其降解,从而增强肿瘤细胞的侵袭能力。LR1可能在正常妊娠和葡萄胎妊娠中控制滋养层细胞侵袭方面发挥作用。

材料与方法

对17例孕周匹配的正常胎盘、10例完全性葡萄胎(CM)和4例部分性葡萄胎(PM)的总cDNA进行实时聚合酶链反应(RT-PCR)。对17例孕周匹配的胎盘、17例PM和19例CM制备的石蜡切片进行LR1的免疫定位。

结果

RT-PCR显示,与正常胎盘相比,葡萄胎组织(PM和CM合并)中LR1 mRNA表达增加了13倍(p = 0.012)。免疫组织化学分析显示LR1定位于蜕膜细胞。在正常胎盘中,LR1定位于蜕膜细胞膜。然而,在PM和CM中,在蜕膜细胞的细胞质中也发现了LR1。有趣的是,通过免疫组织化学方法,我们发现PM中LR1的蛋白表达高于正常胎盘或CM(分别为p = 0.001和p = 0.024)。

结论

LR1在正常胎盘和葡萄胎(CM和PM)的蜕膜细胞中均有表达。CM和PM中的蜕膜细胞表达LR1明显高于胎盘中的蜕膜细胞。葡萄胎组织与母体子宫内膜中LR1表达增强之间的潜在机制尚不清楚。

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