Publications by authors named "J Visvader"

Hepatocytes are organized into distinct zonal subsets across the liver lobule, yet their contributions to liver homeostasis and regeneration remain controversial. Here, we developed multiple genetic lineage-tracing mouse models to systematically address this. We found that the liver lobule can be divided into two major zonal and molecular hepatocyte populations marked by Cyp2e1 or Gls2.

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Hormone-receptor-positive (HR) luminal cells largely mediate the response to estrogen and progesterone during mammary gland morphogenesis. However, there remains a lack of consensus on the precise nature of the precursor cells that maintain this essential HR lineage. Here we refine the identification of HR progenitors and demonstrate their unique regenerative capacity compared to mature HR cells.

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Article Synopsis
  • Breast cancer's complexity necessitates a deeper understanding of cellular diversity to improve treatment methods, particularly by studying genetic variations in its subtypes at a single-cell level.
  • This study integrates single-cell RNA sequencing from various sources, resulting in a diverse dataset of 117 samples, which include different breast cancer subtypes like HR+, HER2+, and TNBC, to analyze similarities and differences across models.
  • Results show that PDX models better reflect patient samples than TNBC cell lines, with therapeutic efficacy linked to subtype proportions, underscoring the importance of these findings for preclinical research decisions in breast cancer treatment development.*
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Despite aging being one of the strongest risk factors for cancer, little is known about the biological mechanisms that promote tumor initiation. In this issue of Cancer Cell, Yan et al. address this fundamental question in the context of breast cancer and report that midkine is upregulated during the aging process and can promote tumorigenesis.

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The transcription factor EHF is highly expressed in the lactating mammary gland, but its role in mammary development and tumorigenesis is not fully understood. Utilizing a mouse model of Ehf deletion, herein, we demonstrate that loss of Ehf impairs mammary lobuloalveolar differentiation at late pregnancy, indicated by significantly reduced levels of milk genes and milk lipids, fewer differentiated alveolar cells, and an accumulation of alveolar progenitor cells. Further, deletion of Ehf increased proliferative capacity and attenuated prolactin-induced alveolar differentiation in mammary organoids.

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