首页> 美国卫生研究院文献>other >15-Deoxy-Δ1214-Prostaglandin J2 Inhibits Osteolytic Breast Cancer Bone Metastasis and Estrogen Deficiency-Induced Bone Loss
【2h】

15-Deoxy-Δ1214-Prostaglandin J2 Inhibits Osteolytic Breast Cancer Bone Metastasis and Estrogen Deficiency-Induced Bone Loss

机译:15-脱氧-Δ1214-前列腺素J2抑制溶骨性乳腺癌骨转移和雌激素缺乏症引起的骨丢失。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Breast cancer is the major cause of cancer death in women worldwide. The most common site of metastasis is bone. Bone metastases obstruct the normal bone remodeling process and aberrantly enhance osteoclast-mediated bone resorption, which results in osteolytic lesions. 15-deoxy-Δ12,14-prostaglandin J2 (15d-PGJ2) is an endogenous ligand of peroxisome proliferator-activated receptor gamma (PPARγ) that has anti-inflammatory and antitumor activity at micromolar concentrations through PPARγ-dependent and/or PPARγ-independent pathways. We investigated the inhibitory activity of 15d-PGJ2 on the bone loss that is associated with breast cancer bone metastasis and estrogen deficiency caused by cancer treatment. 15d-PGJ2 dose-dependently inhibited viability, migration, invasion, and parathyroid hormone-related protein (PTHrP) production in MDA-MB-231 breast cancer cells. 15d-PGJ2 suppressed receptor activator of nuclear factor kappa-B ligand (RANKL) mRNA levels and normalized osteoprotegerin (OPG) mRNA levels in hFOB1.19 osteoblastic cells treated with culture medium from MDA-MB-231 cells or PTHrP, which decreased the RANKL/OPG ratio. 15d-PGJ2 blocked RANKL-induced osteoclastogenesis and inhibited the formation of resorption pits by decreasing the activities of cathepsin K and matrix metalloproteinases, which are secreted by mature osteoclasts. 15d-PGJ2 exerted its effects on breast cancer and bone cells via PPARγ-independent pathways. In Balb/c nuu mice that received an intracardiac injection of MDA-MB-231 cells, subcutaneously injected 15d-PGJ2 substantially decreased metastatic progression, cancer cell-mediated bone destruction in femora, tibiae, and mandibles, and serum PTHrP levels. 15d-PGJ2 prevented the destruction of femoral trabecular structures in estrogen-deprived ICR mice as measured by bone morphometric parameters and serum biochemical data. Therefore, 15d-PGJ2 may be beneficial for the prevention and treatment of breast cancer-associated bone diseases.
机译:乳腺癌是全世界女性癌症死亡的主要原因。最常见的转移部位是骨骼。骨转移会阻碍正常的骨重塑过程,并异常增强破骨细胞介导的骨吸收,从而导致溶骨性病变。 15-脱氧-Δ 12,14 -前列腺素J2(15d-PGJ2)是过氧化物酶体增殖物激活受体γ(PPARγ)的内源性配体,在通过PPARγ的微摩尔浓度下具有抗炎和抗肿瘤活性依赖性和/或PPARγ非依赖性途径。我们研究了15d-PGJ2对与乳腺癌骨转移和癌症治疗引起的雌激素缺乏有关的骨丢失的抑制活性。 15d-PGJ2剂量依赖性地抑制MDA-MB-231乳腺癌细胞中的活力,迁移,侵袭和甲状旁腺激素相关蛋白(PTHrP)的产生。 15d-PGJ2抑制了用MDA-MB-231细胞或PTHrP培养基处理的hFOB1.19成骨细胞中核因子kB-B配体(RANKL)mRNA水平和正常骨保护素(OPG)mRNA水平的受体激活剂,从而降低了RANKL / OPG比。 15d-PGJ2通过降低组织蛋白酶K和基质金属蛋白酶的活性来阻止RANKL诱导的破骨细胞生成,并抑制吸收坑的形成,而后者由成熟破骨细胞分泌。 15d-PGJ2通过不依赖PPARγ的途径对乳腺癌和骨细胞发挥作用。在接受心内注射MDA-MB-231细胞的Balb / c nu / nu小鼠中,皮下注射15d-PGJ2大大降低了转移进程,癌细胞介导的股骨,胫骨和下颌骨破坏以及血清PTHrP水平。通过骨形态参数和血清生化数据测定,15d-PGJ2可防止雌激素剥夺的ICR小鼠破坏股骨小梁结构。因此,15d-PGJ2可能对预防和治疗与乳腺癌有关的骨病有益。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号