سامانه مدیریت نشریات علمی دانشگاه علوم پزشکی مشهد

Rasooli Tehrani, Reihane, Asgarian-Omran, Hossein, Taghiloo, Saeid, Valadan, Reza, Azizi, Soheil, Ajami, Abolghasem. (1403). Infiltration of innate and adoptive lymphoid cells in 4T1 and MC4-L2 breast cancer models. , 28(1), 63-71. doi: 10.22038/ijbms.2024.80535.17434
Reihane Rasooli Tehrani; Hossein Asgarian-Omran; Saeid Taghiloo; Reza Valadan; Soheil Azizi; Abolghasem Ajami. "Infiltration of innate and adoptive lymphoid cells in 4T1 and MC4-L2 breast cancer models". , 28, 1, 1403, 63-71. doi: 10.22038/ijbms.2024.80535.17434
Rasooli Tehrani, Reihane, Asgarian-Omran, Hossein, Taghiloo, Saeid, Valadan, Reza, Azizi, Soheil, Ajami, Abolghasem. (1403). 'Infiltration of innate and adoptive lymphoid cells in 4T1 and MC4-L2 breast cancer models', , 28(1), pp. 63-71. doi: 10.22038/ijbms.2024.80535.17434
Rasooli Tehrani, Reihane, Asgarian-Omran, Hossein, Taghiloo, Saeid, Valadan, Reza, Azizi, Soheil, Ajami, Abolghasem. Infiltration of innate and adoptive lymphoid cells in 4T1 and MC4-L2 breast cancer models. , 1403; 28(1): 63-71. doi: 10.22038/ijbms.2024.80535.17434

Infiltration of innate and adoptive lymphoid cells in 4T1 and MC4-L2 breast cancer models

Iranian Journal of Basic Medical Sciences
مقاله 8، دوره 28، شماره 1، فروردین 2025، صفحه 63-71    اصل مقاله (597.65 K)
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.22038/ijbms.2024.80535.17434
نویسندگان
Reihane Rasooli Tehrani1؛ Hossein Asgarian-Omran1، 2؛ Saeid Taghiloo1؛ Reza Valadan1، 3؛ Soheil Azizi4؛ Abolghasem Ajami* 1، 3
1Department of Medical Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
2Gastrointestinal Cancer Research Center, Mazandaran University of Medical Sciences, Sari, Iran
3Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Sari, Iran
4Department of Laboratory Sciences, Faculty of Paramedicine, Mazandaran University of Medical Sciences, Sari, Iran
چکیده
Objective(s): Innate lymphoid cells (ILCs) are tissue-resident lymphocytes that have vital roles in activating further immune responses. However, due to their tumor-induced diversity, we decided to examine ILCs, T cells, and the associated cytokines in mouse models of breast cancer.
Materials and Methods: 4T1 and MC4-L2 cells were used to induce triple-negative and hormone-receptor-positive breast cancer, respectively. Tumor tissue was resected at early and late stages of tumor growth and used for further analysis. Total RNA was extracted and used in Real-Time PCR to analyze the expression of IFN-γ, IL-4, IL-10, IL-13, and IL-22. Tumor tissue was digested and used in a flow cytometric assay. H&E staining was used to examine the pathology of tumor progression.  
Results: Both tumor models showed a notable increase in T-cell frequency at the early stage of tumor growth. However, as the tumors progressed, the frequency of T cells significantly decreased, while the ILC component exhibited a significant increase in tumor progression. Gene analysis indicated a significant increase in the inflammatory to anti-inflammatory cytokine ratio during tumor progression in the tumor model. In contrast, this ratio was considerably reduced in advanced MC4-L2 tumors. Both tumor models showed the development of invasive breast carcinoma and lung metastasis in advanced tumors.
Conclusion: Our study highlighted the expansion of ILCs during tumor progression in two distinct breast cancer models with different immunogenicity. These findings suggest that ILCs may actively modulate the tumor microenvironment during the advanced stage of tumor growth.
کلیدواژه‌ها
4T1؛ Breast cancer؛ CD4+ T-lymphocytes؛ CD8+ T-lymphocytes؛ Innate lymphoid cells؛ MC4-L2
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