Literature DB >> 16919866

Combined phospho-Akt and PTEN expressions associated with post-treatment hysterectomy after conservative progestin therapy in complex atypical hyperplasia and stage Ia, G1 adenocarcinoma of the endometrium.

Takeo Minaguchi1, Shunsuke Nakagawa, Yutaka Takazawa, Tomomi Nei, Koji Horie, Toshihiro Fujiwara, Yutaka Osuga, Toshiharu Yasugi, Koji Kugu, Tetsu Yano, Hiroyuki Yoshikawa, Yuji Taketani.   

Abstract

Young patients with complex atypical hyperplasia (CAH) or stage Ia, G1 adenocarcinoma (IaG1) of the endometrium, who desire to preserve fertility, can select the conservative therapy by oral progestin, medroxyprogesterone acetate (MPA). However, conservative treatments involve potential risks of progression and recurrence. In an attempt to find out molecular markers for sensitivity to MPA, we performed immunohistochemical analysis of PTEN, phospho-Akt, p53, ER and PgR in MPA-treated 31 cases with CAH or IaG1. Eleven of 12 cases (92%) with CAH and 15 of 19 cases (79%) with IaG1 demonstrated an initial complete response, while five patients underwent hysterectomy due to no response. Four of 11 responders (36%) with CAH and five of 15 responders (33%) with IaG1 later developed relapse. Five of nine patients (56%) with CAH and three of 11 patients (27%) with IaG1 became pregnant after infertility treatment. Immunohistochemical analysis revealed that phospho-Akt expression was significantly decreased by MPA administration (p=0.002). Furthermore, combination of two factors, weak phosho-Akt or PTEN-null expression, was found to be significantly associated with receiving hysterectomy (p=0.04), while each factor showed a trend without statistical significance (p=0.07 and 0.2, respectively). Strong expression of both ER and PgR significantly correlated with successful pregnancy after infertility treatment following complete response to MPA (p=0.02). Our observations in vivo suggest that anti-tumor action of MPA may be mediated by dephosphorylation of Akt, and that immunohistochemical evaluation of phospho-Akt and PTEN may be able to predict the outcome of MPA therapy.

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Year:  2006        PMID: 16919866     DOI: 10.1016/j.canlet.2006.06.013

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  19 in total

1.  Biomarkers of progestin therapy resistance and endometrial hyperplasia progression.

Authors:  Kristen Upson; Kimberly H Allison; Susan D Reed; Carolyn D Jordan; Katherine M Newton; Elizabeth M Swisher; Jennifer A Doherty; Rochelle L Garcia
Journal:  Am J Obstet Gynecol       Date:  2012-05-16       Impact factor: 8.661

2.  All-cause mortality in young women with endometrial cancer receiving progesterone therapy.

Authors:  Maria P Ruiz; Yongmei Huang; June Y Hou; Ana I Tergas; William M Burke; Cande V Ananth; Alfred I Neugut; Dawn L Hershman; Jason D Wright
Journal:  Am J Obstet Gynecol       Date:  2017-08-24       Impact factor: 8.661

3.  Histologic effects of medroxyprogesterone acetate on endometrioid endometrial adenocarcinoma: a Gynecologic Oncology Group study.

Authors:  Richard J Zaino; William E Brady; William Todd; Kimberly Leslie; Edgar G Fischer; Neil S Horowitz; Robert S Mannel; Joan L Walker; Marina Ivanovic; Linda R Duska
Journal:  Int J Gynecol Pathol       Date:  2014-11       Impact factor: 2.762

4.  Progesterone receptor signaling in the microenvironment of endometrial cancer influences its response to hormonal therapy.

Authors:  Deanna M Janzen; Miguel A Rosales; Daniel Y Paik; Daniel S Lee; Daniel A Smith; Owen N Witte; M Luisa Iruela-Arispe; Sanaz Memarzadeh
Journal:  Cancer Res       Date:  2013-06-06       Impact factor: 12.701

5.  Expression of thyroid transcription factor-1 in normal endometrium is associated with risk of endometrial cancer development.

Authors:  Peggy S Sullivan; Erin L Maresh; David B Seligson; Omar Habeeb; Madhuri Wadehra; Lee Goodglick; Oliver Dorigo
Journal:  Mod Pathol       Date:  2012-03-30       Impact factor: 7.842

6.  Mig-6 suppresses endometrial cancer associated with Pten deficiency and ERK activation.

Authors:  Tae Hoon Kim; Jung-Yoon Yoo; Hong Im Kim; Jenifer Gilbert; Bon Jeong Ku; Jane Li; Gordon B Mills; Russell R Broaddus; John P Lydon; Jeong Mook Lim; Ho-Geun Yoon; Jae-Wook Jeong
Journal:  Cancer Res       Date:  2014-11-06       Impact factor: 12.701

7.  Cell-autonomous activation of the PI3-kinase pathway initiates endometrial cancer from adult uterine epithelium.

Authors:  Sanaz Memarzadeh; Yang Zong; Deanna M Janzen; Andrew S Goldstein; Donghui Cheng; Takeshi Kurita; Amanda M Schafenacker; Jiaoti Huang; Owen N Witte
Journal:  Proc Natl Acad Sci U S A       Date:  2010-09-20       Impact factor: 11.205

8.  The oncogenic mutation in the pleckstrin homology domain of AKT1 in endometrial carcinomas.

Authors:  K Shoji; K Oda; S Nakagawa; S Hosokawa; G Nagae; Y Uehara; K Sone; Y Miyamoto; H Hiraike; O Hiraike-Wada; T Nei; K Kawana; H Kuramoto; H Aburatani; T Yano; Y Taketani
Journal:  Br J Cancer       Date:  2009-06-02       Impact factor: 7.640

9.  Phosphatase and tensin homologue deleted on chromosome 10.

Authors:  Imran Haruna Abdulkareem; Maria Blair
Journal:  Niger Med J       Date:  2013-03

Review 10.  Preserving fertility in young patients with endometrial cancer: current perspectives.

Authors:  Eleftheria Kalogera; Sean C Dowdy; Jamie N Bakkum-Gamez
Journal:  Int J Womens Health       Date:  2014-07-29
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