Establishment of the PDTX model of gynecological tumors

Wen Yang1, Wen-Sheng Fan1, Ming-Xia Ye1

  • 1Department of Obstetrics and Gynecology, Chinese PLA General Hospital 28 Fuxing Road, Haidian District, Beijing 100853, China.

Abstract

Insights

Patient-derived tumor xenograft (PDTX) models were established from gynecological tumors in NCG mice. These models accurately reflect patient tumor pathology, aiding in personalized treatment and research.

Area of Science:

  • Oncology
  • Translational Medicine
  • Animal Models

Background:

  • Gynecological tumors present a significant health challenge.
  • Effective preclinical models are crucial for advancing treatment strategies.
  • Patient-derived tumor xenografts (PDTX) offer a promising avenue for personalized medicine.

Purpose of the Study:

  • To establish and validate a PDTX model for gynecological tumors.
  • To assess the fidelity of the PDTX model compared to original patient tumors.
  • To evaluate the utility of the PDTX model for guiding gynecological cancer treatment and research.

Main Methods:

  • Fresh tumor tissues from 15 gynecological cancer patients were xenografted into NOD-Prkdcem26ll2rgem26Nju (NCG) mice.
  • Tumor formation rate, latency, volume, invasion, and metastasis were monitored.
  • Pathological H&E staining and pharmacodynamic testing were performed to assess model consistency and utility.

Main Results:

  • A 46.7% success rate was achieved in establishing 7 out of 15 PDTX models.
  • Tumor formation occurred between 21-130 days (median 73 days).
  • The established PDTX models retained the differentiation, morphology, and structural characteristics of the original tumors, with successful pharmacodynamic testing in five cases.

Conclusions:

  • The developed PDTX model demonstrates high consistency with patient tumor pathology.
  • PDTX models serve as a valuable substitute for clinical patients in gynecological oncology research.
  • These models can guide accurate treatment decisions and facilitate scientific advancements in gynecological tumors.

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