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Loss of LOXL2 Promotes Uterine Hypertrophy and Tumor Progression by Enhancing H3K36ac-Dependent Gene Expression.

Xufeng LuDazhuan E XinJuanjuan K DuQuanli C ZouQian WuYanan S ZhangWenhai DengJicheng YueXing S FanYuanyuan ZengXiaju ChengXue S LiZhaoyuan HouMan MohanTing C ZhaoXiaomei LuZhijie ChangLi-Yan XuYu SunXiongbing ZuYu ZhangY Eugene Chinn
Published in: Cancer research (2022)
LOXL2 loss reprograms the epigenetic landscape to promote uterine cancer initiation and progression and repress the efficacy of anti-PD-1 immunotherapy, indicating that LOXL2 is a tumor suppressor.
Keyphrases
  • gene expression
  • dna methylation
  • papillary thyroid
  • poor prognosis
  • squamous cell
  • single cell
  • squamous cell carcinoma