Establishment of a patient-derived drug-resistant oral squamous cell carcinoma animal model

Chuanni Feng , Hao Liu , Yalan Lu , Yanfeng Xu , Xinghan Wu , Jinlong Wang , Chuan Qin , Binbin Li , Yanhong Li

Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (8) : 1513 -1523.

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Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (8) :1513 -1523. DOI: 10.1002/ame2.70066
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Establishment of a patient-derived drug-resistant oral squamous cell carcinoma animal model

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Abstract

Oral squamous cell carcinoma (OSCC) constitutes 90% of oral tumors. Advanced cases severely impair patients' life quality of life due to anatomical location and limited therapies. Conventional treatments often induce drug resistance or recurrence. Patient-derived xenograft (PDX) models are widely used to simulate tumor progression and drug responses, serving as translational tools for precision medicine. This study aimed to establish drug-resistant OSCC PDX models. Human OSCC tissues were transplanted into immunodeficient mice and passaged (P1–P2). At P2 (tumor volume: 40–80 mm3), mice received cisplatin (1 mg/kg, three times/week) with cetuximab (1 mg/kg, weekly), GSK690693 (10 mg/kg, five times/week), or rapamycin (4 mg/kg, five times/week). PDX tissues from groups with less-therapeutic response (manifested as larger tumor volumes) were serially passaged to assess treatment efficacy. Tumor tissues with diminished drug sensitivity underwent histopathological analysis and identified stability of their tumor characteristics using hematoxylin–eosin (HE) and immunohistochemical staining after one additional passage and retreatment. Results demonstrated that successive passaging accelerates tumor growth. First-generation treatments showed universal sensitivity. At P2, cisplatin–cetuximab and rapamycin groups remained sensitive, whereas GSK690693 efficacy declined. Continued passaging of GSK690693-treated tumors confirmed resistance, as evidenced by exhibiting enhanced malignant characteristics at histological level. The GSK690693-resistant model was established first, whereas resistant models of other treatment groups were established according to similar protocols. These findings suggest that sequential passaging and drug exposure in PDX models recapitulated clinical tumor evolution, enabling the development of drug-resistant OSCC models. This study can offer methodological insights for precision therapy of OSCC.

Keywords

drug resistance / oral squamous cell carcinoma / PDX model / precision therapy / successive passaging

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Chuanni Feng, Hao Liu, Yalan Lu, Yanfeng Xu, Xinghan Wu, Jinlong Wang, Chuan Qin, Binbin Li, Yanhong Li. Establishment of a patient-derived drug-resistant oral squamous cell carcinoma animal model. Animal Models and Experimental Medicine, 2025, 8(8): 1513-1523 DOI:10.1002/ame2.70066

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References

[1]

Ilie IO, Mărgăritescu OC, Stepan AE, et al. Epidemiological and histopathological features of oral squamous cell carcinoma-a retrospective study. Curr Health Sci J. 2024; 50(3): 411-420.

[2]

Mordzińska-Rak A, Telejko I, Adamczuk G, Trombik T, Stepulak A, Błaszczak E. Advancing head and neck cancer therapies: from conventional treatments to emerging strategies. Biomedicine. 2025; 13(5): 1046.

[3]

Alshwayyat S, Alawneh A, Kamal H, et al. Personalized therapeutic strategies and prognosis for advanced laryngeal squamous cell carcinoma: insights from machine learning models. Am J Otolaryngol. 2025; 46(4): 104633.

[4]

Machtay M, Torres-Saavedra PA, Thorstad W, et al. Postoperative radiotherapy ± cetuximab for intermediate-risk head and neck cancer. J Clin Oncol. 2025; 43(12): 1474-1487.

[5]

Hanna GJ, Oakley LB, Shi R, et al. Duvelisib with docetaxel for patients with anti-PD-1 refractory, recurrent, or metastatic head and neck squamous cell carcinoma. Clin Cancer Res. 2025; 31(4): 619-627.

[6]

Becker AS, Klauk F, Freitag T, et al. Inhibition of platin-induced BCL2 increase overcomes chemoresistance in squamous cell carcinoma of the head and neck through resensitization to cell death. Transl Oncol. 2025; 53: 102308.

[7]

Kang SH, Oh SY, Lee KY, et al. Differential effect of cancer-associated fibroblast-derived extracellular vesicles on cisplatin resistance in oral squamous cell carcinoma via miR-876-3p. Theranostics. 2024; 14(2): 460-479.

[8]

Karimian A, Mir SM, Parsian H, et al. Crosstalk between phosphoinositide 3-kinase/Akt signaling pathway with DNA damage response andoxidative stress in cancer. J Cell Biochem. 2019; 120: 10248-10272.

[9]

Liu J, Duan Z, Guo W, et al. Targeting the BRD4/FOXO3a/CDK6 axis sensitizes AKT inhibition in luminal breast cancer. Nat Commun. 2018; 9(1): 5200.

[10]

Makhov PB, Golovine K, Kutikov A, et al. Modulation of Akt/mTOR signaling overcomes sunitinib resistance in renal and prostate cancer cells. Mol Cancer Ther. 2012; 11(7): 1510-1517.

[11]

Khera N, Rajkumar AS, Abdulkader M, et al. Identification of multidrug chemoresistant genes in head and neck squamous cell carcinoma cells. Mol Cancer. 2023; 22(1): 146.

[12]

Griso AB, Acero-Riaguas L, Castelo B, Cebrián-Carretero JL, Sastre-Perona A. Mechanisms of cisplatin resistance in HPV negative head and neck squamous cell carcinomas. Cells. 2022; 11(3): 561.

[13]

Jamal-Hanjani M, Wilson GA, McGranahan N, et al. Tracking the evolution of non-small-cell lung cancer. N Engl J Med. 2017; 376: 2109-2121.

[14]

Cai W, Lin D, Wu C, et al. Intratumoral heterogeneity of ALK-rearranged and ALK/EGFR coaltered lung adenocarcinoma. J Clin Oncol. 2015; 33(32): 3701-3709.

[15]

Shao Y, Zhong DS. Histological transformation after acquired resistance to epidermal growth factor tyrosine kinase inhibitors. Int J Clin Oncol. 2018; 23: 235-242.

[16]

Zhou J, Liu C, Amornphimoltham P, et al. Mouse models for head and neck squamous cell carcinoma. J Dent Res. 2024; 103(6): 585-595.

[17]

Jung J, Seol HS, Chang S. The generation and application of patient-derived xenograft model for cancer research. Cancer Res Treat. 2018; 50(1): 1-10.

[18]

Krumbach R, Schuler J, Hofmann M, et al. Primary resistance to cetuximab in a panel of patient-derived tumour xenograft models: activation of MET as one mechanism for drug resistance. Eur J Cancer. 2011; 47(8): 1231-1243.

[19]

Zanella ER, Grassi E, Trusolino L. Towards precision oncology with patient-derived xenografts. Nat Rev Clin Oncol. 2022; 19(11): 719-732.

[20]

Guillen KP, Fujita M, Butterfield AJ, et al. A human breast cancer-derived xenograft and organoid platform for drug discovery and precision oncology. Nat Cancer. 2022; 3(2): 232-250.

[21]

Li B, Li J, Xu WW, et al. Suppression of esophageal tumor growth and chemoresistance by directly targeting the PI3K/AKT pathway. Oncotarget. 2014; 5(22): 11576-11587.

[22]

Strom TJ, Trotti AM, Kish J, et al. Comparison of every 3 week cisplatin or weekly cetuximab with concurrent radiotherapy for locally advanced head and neck cancer. Oral Oncol. 2015; 51(7): 704-708.

[23]

De Velasco MA, Kura Y, Ando N, et al. Context-specific efficacy of Apalutamide therapy in preclinical models of Pten-deficient prostate cancer. Cancers (Basel). 2021; 13(16): 3975.

[24]

Qiu S, Li Y, Liu F. Standardized treatment of oral cancer under the guidance of clinical practice guidelines of National Comprehensive Cancer Network. Hua Xi Kou Qiang Yi Xue Za Zhi. 2024; 42(5): 566-571. (English, Chinese).

[25]

Aparicio S, Hidalgo M, Kung AL. Examining the utility of patient-derived xenograft mouse models. Nat Rev Cancer. 2015; 15(5): 311-316.

[26]

Bailey C, Black JRM, Reading JL, et al. Tracking cancer evolution through the disease course. Cancer Discov. 2021; 11(4): 916-932.

[27]

Kiang KMY, Chan AA, Leung GKK. Secondary gliosarcoma: the clinicopathological features and the development of a patient-derived xenograft model of gliosarcoma. BMC Cancer. 2021; 21(1): 265.

[28]

Ben-David U, Ha G, Tseng YY, et al. Patient-derived xenografts undergo murine-specific tumor evolution. Nat Genet. 2017; 49: 1567-1575.

[29]

Fuchs V, Sobarzo A, Msamra M, et al. Personalizing non-small cell lung cancer treatment through patient-derived xenograft models: preclinical and clinical factors for consideration. Clin Transl Oncol. 2024; 26(9): 2227-2239.

[30]

Derose YS, Wang G, Lin YC, et al. Tumor grafts derived from women with breast cancer authentically reflect tumor pathology, growth, metastasis and disease outcomes. Nat Med. 2011; 17(11): 1514-1520.

[31]

Yao Y, Wang Y, Chen L, et al. Clinical utility of PDX cohorts to reveal biomarkers of intrinsic resistance and clonal architecture changes underlying acquired resistance to cetuximab in HNSCC. Signal Transduct Target Ther. 2022; 7(1): 73.

[32]

Campbell KM, Lin T, Zolkind P, et al. Oral cavity squamous cell carcinoma xenografts retain complex genotypes and Intertumor molecular heterogeneity. Cell Rep. 2018; 24(8): 2167-2178.

[33]

Kreso A, O'Brien CA, Van Galen P, et al. Variable clonal repopulation dynamics influence chemotherapy response in colorectal cancer. Science. 2013; 339(6119): 543-548.

[34]

Garralda E, Paz K, Lopez-Casas PP, et al. Integrated next-generation sequencing and avatar mouse models for personalized cancer treatment. Clin Cancer Res. 2014; 20(9): 2476-2484.

[35]

Eerew P, Steif A, Khattra J, et al. Dynamics of genomic clones in breast cancer patient xenografts at single-cell resolution. Nature. 2015; 518(7539): 422-426.

[36]

Morelli MP, Calvo E, Ordonez E, et al. Prioritizing phase I treatment options through preclinical testing on personalized tumorgraft. J Clin Oncol. 2012; 30(4): e45-e48.

[37]

Boven E. Phase II preclinical drug screening in human tumor xenografts: a first European multicenter collaborative study. Cancer Res. 1992; 52: 5940-5947.

[38]

Lee J-K. Pharmacogenomic landscape of patient-derived tumor cells informs precision oncology therapy. Nat Genet. 2018; 50: 1399-1411.

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2025 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.

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