Publications by authors named "Zhaochang Qi"

Article Synopsis
  • - Approximately 70% of breast cancer cases are luminal-type (ER+), which can be treated with tamoxifen, but 30% of these patients develop resistance, mainly due to the activation of the PI3K pathway.
  • - Research found that N6 adenine-specific DNA methyltransferase 1 (N6AMT1) is highly expressed in luminal breast cancer but decreased in tamoxifen-resistant cells, with FOXA1 promoting N6AMT1 transcription.
  • - Increasing N6AMT1 expression restores tamoxifen sensitivity in resistant cells, and combining tamoxifen with a p110α inhibitor enhances treatment effectiveness, suggesting that N6AMT1 could serve as a biomarker
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Background: Mammalian enabled (MENA) protein is a member of the enabled/vasodilator stimulated phosphoprotein (Ena/VASP) protein family, which regulates cytoplasmic actin network assembly. It plays a significant role in breast cancer invasion, migration, and resistance against targeted therapy and chemotherapy. However, its role in the efficacy of endocrine therapy for the hormone receptor-positive (HR) breast cancer patients is not known.

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Treatment of acute pancreatitis (AP) and chronic pancreatitis (CP) remains problematic due to a lack of knowledge about disease-specific regulatory targets and mechanisms. The purpose of this study was to screen proteins related to endoplasmic reticulum (ER) stress and apoptosis pathways that may play a role in pancreatitis. Human pancreatic tissues including AP, CP, and healthy volunteers were collected during surgery.

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Chronic pancreatitis (CP) is a progressive, recurrent inflammatory disorder of the pancreas. Initiation and progression of CP can result from serine protease 1 (PRSS1) overaccumulation and the ensuing endoplasmic reticulum (ER) stress. However, how ER stress pathways regulate the development and progression of CP remains poorly understood.

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