EN
×
EN
在线咨询
在线
咨询
电话
电话
微信公众号
业务咨询
中国:
业务咨询专线:400-780-8018
(仅限服务咨询,其他事宜请拨打川沙总部电话)
川沙总部电话: +86 (21) 5859-1500
海外:
+1(781)535-1428(U.S.)
0044 7790 816 954 (Europe)
留言
留言
在线留言×
点击切换
Customer Center
客户中心

title">端锚聚合酶抑制剂G007-LK具有治疗结直肠癌的潜力,本研究中PK实验通过美迪西进行

2025-07-11
|
访问量:

Colorectal tumors, in particular, often show dysregulated WNT/β-catenin signalling. G007-LK may be a candidate for use in preclinical trials to determine the efficacy of this drug in preventing growth of WNT dependent tumors. Doses of the tankyrase inhibitor G007-LK shown to be sufficient to inhibit tumor growth are well tolerated by mice within the time frames investigated. Lineage tracing from LGR5+ intestinal stem cells was reduced upon G007-LK treatment, without altering the main morphological characteristics of the intestine. Moreover, mice treated with G007-LK did not experience weight loss, suggesting that the absorptive capacity of the intestine was not negatively impacted.

Medicilon Preclinical Research LCC performed the pharmacokinetic studies.

93.pngReference:

Jens Henrik Norum, et al. The tankyrase inhibitor G007-LK inhibits small intestine LGR5+ stem cell proliferation without altering tissue morphology. Biol Res. 2018 Jan 9;51(1):3. doi: 10.1186/s40659-017-0151-6.


相关新闻
×
搜索验证
点击切换
百度 搜狗 360搜索 顾村言|书迹心迹——关于刘海粟与苏东坡 杜邦中国涉嫌违反反垄断法被立案 10后的生死观还是太超前了 美股2天暴跌47万亿 韩国政局何去何从

      <code id='4cb52'></code><style id='b72c5'></style>
    • <acronym id='b2f7c'></acronym>
      <center id='ddc83'><center id='7f90c'><tfoot id='065b9'></tfoot></center><abbr id='ab5dd'><dir id='3d871'><tfoot id='1fed7'></tfoot><noframes id='02cbf'>

    • <optgroup id='44d18'><strike id='62fab'><sup id='250e1'></sup></strike><code id='f32b0'></code></optgroup>
        1. <b id='c0947'><label id='2f0b4'><select id='784d4'><dt id='c7d30'><span id='d982f'></span></dt></select></label></b><u id='77004'></u>
          <i id='a6df2'><strike id='4c269'><tt id='fb2a5'><pre id='77491'></pre></tt></strike></i>