Establishment and evaluation of a lung metastasis model of colorectal cancer in experimental animals

Authors

  • Д.Анужин АШУҮИС, Био-АС, Анатомийн тэнхим Author
  • Б.Маналжав АШУҮИС, Sci-lab клубийн оюутан Author
  • М.Барсболд АШУҮИС, Sci-lab клубийн оюутан Author
  • Ч.Алтанчимэг АШУҮИС, Sci-lab клубийн оюутан Author
  • Б.Отгонсүрэн АШУҮИС, Sci-lab клубийн оюутан Author
  • Т.Хүсэлт-Од АШУҮИС, Био-АС-ийн оюутан Author
  • Ү.Сувд-Эрдэнэ АШУҮИС, Био-АС-ийн оюутан Author
  • Л.Энхсайхан АШУҮИС, Био-АС, Дархлаа судлалын тэнхим , АШУҮИС, Био-Анагаахын Хүрээлэн Author
  • Ч.Гансүх АШУҮИС, Био-АС, Дархлаа судлалын тэнхим Author
  • Б.Журамт АШУҮИС, Био-АС, Анатомийн тэнхим Author

Keywords:

Experimental animal model, Lung, C57BL/6J mouse, MC38

Abstract

Background: Currently, colorectal cancer (CRC) ranks as the third most common cancer and the second leading cause of cancer-related mortality worldwide. CRC frequently metastasizes to the liver (50%), lungs (10–15%), peritoneum (4%), bones (10.7%–23.7%), brain (0.3%–6%), and spinal cord. Approximately 35% of CRC cases are diagnosed before distant metastasis, 36% upon lymph node involvement, and 23% after distant organ metastasis. Although several studies have established primary tumor models in mice in our country, there are limited studies on experimental lung metastasis models, prompting the need for this research. Aim: To establish and evaluate a lung metastasis model of colorectal cancer in C57BL/6J mice using the MC38 cell line. Materials and Methods: This study was conducted at the Institute of Biomedical Sciences, Mongolian National University of Medical Sciences. Approval was obtained from the Ethics Review Board of the Mongolian National University of Medical Sciences (2023/3-09) and all laboratory safety regulations and protocols were strictly followed. Male C57BL/6J mice bred at the Experimental Animal Center of Mongolian National University of Medical Sciences were used. MC38 murine colorectal carcinoma cells were cultured and injected intravenously (via the tail vein) at a concentration of 0.25×10⁶ cells per mouse (n=12) to induce lung metastasis. Histological analysis was subsequently performed. Results: Histological examination revealed significant alterations in lung tissue architecture, characterized by areas of dense infiltration by pleomorphic, hyperchromatic cells, disrupting the normal alveolar structure. No histological abnormalities were observed in other organs. Conclusion: Intravenous injection of MC38 colorectal adenocarcinoma cells into the tail vein of C57BL/6J mice successfully induced lung metastases, characterized by hyperchromatic, pleomorphic cell infiltrates forming glandular structures within the lung parenchyma.

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Author research profiles: Т.Хүсэлт-Од, Л.Энхсайхан, Ч.Гансүх, Б.Журамт

Published

2025-05-05

Issue

Section

Original Articles