Preclinical Models of Anal Cancer Combined-Modality Therapy

被引:1
|
作者
Johnson, Hillary R. [1 ]
Gunder, Laura C. [1 ]
Gillette, Amani [2 ]
Sleiman, Hana [1 ,9 ]
Rademacher, Brooks L. [1 ]
Meske, Louise M. [1 ,10 ]
Culberson, Wesley S. [3 ]
Micka, John A. [3 ]
Favreau, Peter [2 ,11 ]
Yao, Evan [1 ]
Matkowskyj, Kristina A. [4 ,5 ,6 ]
Skala, Melissa C. [2 ,5 ]
Carchman, Evie H. [1 ,6 ,7 ,8 ]
机构
[1] Univ Wisconsin Madison, Dept Surg, Madison, WI USA
[2] Morgridge Inst Res, Madison, WI USA
[3] Univ Wisconsin Madison, Sch Med & Publ Hlth, Dept Med Phys, Madison, WI USA
[4] Univ Wisconsin Madison, Dept Pathol & Lab Med, Madison, WI USA
[5] Univ Wisconsin Madison, Dept Biomed Engn, Madison, WI USA
[6] William S Middleton Mem Vet, Madison, WI USA
[7] Univ Wisconsin Madison, Carbone Canc Ctr, Sch Med & Publ Hlth, Madison, WI USA
[8] Univ Wisconsin Madison, Clin Sci Ctr, Dept Surg, Div Colorectal Surg, 600 Highland Ave, Madison, WI 53792 USA
[9] Univ Wisconsin Hosp & Clin, Clin Labs, 600 Highland Ave, Madison, WI 53792 USA
[10] Univ Wisconsin Madison, Environm Hlth & Safety, 21 North Pk St, Madison, WI 53715 USA
[11] Stem Pharm Inc, 5520 Nobel Dr, Madison, WI 53711 USA
关键词
Anal cancer; Cancer treatment; Chemoradiotherapy; mTOR; PI3K; Pik3ca; DISEASE; REVEALS;
D O I
10.1016/j.jss.2023.09.053
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introduction: There have been no significant changes in anal cancer treatment options in 4 decades. In this study, we highlight two preclinical models designed to assess anal cancer treatments. Materials and methods: Transgenic K14E6/E7 mice were treated with 7, 12-dimethylbenz(a) anthracene until anal tumors developed. Mice were treated with localized radiation in addition to chemotherapy (combined-modality therapy [CMT]) and compared to no treatment control (NTC). K14E6/E7 mouse anal spheroids with and without Pik3ca mutations were isolated and treated with vehicle, LY3023414 (LY3) (a drug previously shown to be effective in cancer prevention), CMT, or CMT + LY3. Results: In the in vivo model, there was a significant increase in survival in the CMT group compared to the NTC group (P = 0.0392). In the ex vivo model, there was a significant decrease in the mean diameter of CMT and CMT + LY3-treated spheroids compared to vehicle (P <= 0.0001). For LY3 alone compared to vehicle, there was a statistically significant decrease in spheroid size in the K14E6/E7 group without mutation (P = 0.0004).Conclusions: We have provided proof of concept for two preclinical anal cancer treatment models that allow for the future testing of novel therapies for anal cancer. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:82 / 92
页数:11
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