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<p>The fallopian tube (FT) plays a crucial role in fertility, gynecological health, and high-grade serous ovarian cancer (HGSOC) development. Despite its importance, the spatial transcriptome of the FT’s distinct anatomical regions (fimbria, infundibulum, ampulla, and isthmus) remains underexplored. Using the GeoMx Digital Spatial Profiler (DSP) and a targeted ~1800 gene panel, we analyze premenopausal FT epithelium, identifying region-specific gene expression patterns. Our analysis reveals upregulation of mature ciliated cell markers (<i>FOXJ1</i>, <i>MLF1, SPA17, and CTSS</i>) approaching the fimbria, elevated ROS and apoptosis-related transcripts (<i>TXNIP</i>, <i>PRDX5, BAD, GAS1)</i> in the distal FT, and a switch in cell-cell adhesion transcripts (<i>CDH1</i>, <i>CDH3</i>) along the distal-to-proximal axis. We also provide evidence that MHC-II transcripts in the FT are differentially regulated throughout the menstrual cycle, with lower expression in follicular phase. These results suggest spatially regulated expression of FT transcripts with implications for fertilization and early neoplastic changes contributing to HGSOC.</p>

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Spatial transcriptomic profiling of the human fallopian tube epithelium reveals region-specific gene expression patterns

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年3月29日

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  • Jared Sipes,
  • Sagar Rayamajhi,
  • Leonidas E. Bantis,
  • Rashna Madan,
  • Amrita Mitra,
  • Rajni V. Puri,
  • Mohammod Mahmudur Rahman,
  • Foyez Ahmmed,
  • Harsh B. Pathak,
  • Andrew K. Godwin

摘要

The fallopian tube (FT) plays a crucial role in fertility, gynecological health, and high-grade serous ovarian cancer (HGSOC) development. Despite its importance, the spatial transcriptome of the FT’s distinct anatomical regions (fimbria, infundibulum, ampulla, and isthmus) remains underexplored. Using the GeoMx Digital Spatial Profiler (DSP) and a targeted ~1800 gene panel, we analyze premenopausal FT epithelium, identifying region-specific gene expression patterns. Our analysis reveals upregulation of mature ciliated cell markers (FOXJ1, MLF1, SPA17, and CTSS) approaching the fimbria, elevated ROS and apoptosis-related transcripts (TXNIP, PRDX5, BAD, GAS1) in the distal FT, and a switch in cell-cell adhesion transcripts (CDH1, CDH3) along the distal-to-proximal axis. We also provide evidence that MHC-II transcripts in the FT are differentially regulated throughout the menstrual cycle, with lower expression in follicular phase. These results suggest spatially regulated expression of FT transcripts with implications for fertilization and early neoplastic changes contributing to HGSOC.