Sex Matters–Insights from Testing Drug Efficacy in an Animal Model of Pancreatic Cancer

Cancers Pub Date : 2024-05-16 DOI:10.3390/cancers16101901
Benjamin Schulz, Emily Leitner, Tim Schreiber, Tobias Lindner, Rico Schwarz, Nadine Aboutara, Yixuan Ma, Hugo Murua Escobar, Rupert Palme, Burkhard Hinz, Brigitte Vollmar, Dietmar Zechner
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Abstract

Preclinical studies rarely test the efficacy of therapies in both sexes. The field of oncology is no exception in this regard. In a model of syngeneic, orthotopic, metastasized pancreatic ductal adenocarcinoma we evaluated the impact of sex on pathological features of this disease as well as on the efficacy and possible adverse side effects of a novel, small molecule-based therapy inhibiting KRAS:SOS1, MEK1/2 and PI3K signaling in male and female C57BL/6J mice. Male mice had less tumor infiltration of CD8-positive cells, developed bigger tumors, had more lung metastasis and a lower probability of survival compared to female mice. These more severe pathological features in male animals were accompanied by higher distress at the end of the experiment. The evaluated inhibitors BI-3406, trametinib and BKM120 showed synergistic effects in vitro. This combinatorial therapy reduced tumor weight more efficiently in male animals, although the drug concentrations were similar in the tumors of both sexes. These results underline the importance of sex-specific preclinical research and at the same time provide a solid basis for future studies with the tested compounds.
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性别很重要--在胰腺癌动物模型中测试药物疗效的启示
临床前研究很少对男女两性的治疗效果进行测试。肿瘤学领域也不例外。我们在雌雄 C57BL/6J 小鼠共生、正位、转移的胰腺导管腺癌模型中,评估了性别对该疾病病理特征的影响,以及基于小分子抑制 KRAS:SOS1、MEK1/2 和 PI3K 信号转导的新型疗法对雌雄小鼠疗效和可能出现的不良副作用的影响。与雌性小鼠相比,雄性小鼠的肿瘤浸润CD8阳性细胞较少,肿瘤较大,肺转移较多,存活率较低。雄性小鼠的病理特征更为严重,实验结束时的痛苦程度也更高。所评估的抑制剂 BI-3406、曲美替尼和 BKM120 在体外显示出协同效应。尽管雄性动物和雌性动物肿瘤中的药物浓度相似,但这种组合疗法能更有效地减轻雄性动物的肿瘤重量。这些结果凸显了针对不同性别进行临床前研究的重要性,同时也为今后使用受试化合物进行研究奠定了坚实的基础。
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