Via Pier Capponi 6, 50132 Florence, Italy.
Department of Bioscience, Biotechnology and Biopharmaceutics, University of Bari, 70126 Bari, Italy.
Int J Mol Sci. 2021 Apr 12;22(8):3953. doi: 10.3390/ijms22083953.
Pancreatic ductal adenocarcinoma (PDAC) is one of the deadliest malignancies. Present-day treatments have not shown real improvements in reducing the high mortality rate and the short survival of the disease. The average survival is less than 5% after 5 years. New innovative treatments are necessary to curtail the situation. The very dense pancreatic cancer stroma is a barrier that impedes the access of chemotherapeutic drugs and at the same time establishes a pro-proliferative symbiosis with the tumor, thus targeting the stroma has been suggested by many authors. No ideal drug or drug combination for this targeting has been found as yet. With this goal in mind, here we have explored a different complementary treatment based on abundant previous publications on repurposed drugs. The cell surface protein CD44 is the main receptor for hyaluronan binding. Many malignant tumors show over-expression/over-activity of both. This is particularly significant in pancreatic cancer. The independent inhibition of hyaluronan-producing cells, hyaluronan synthesis, and/or CD44 expression, has been found to decrease the tumor cell's proliferation, motility, invasion, and metastatic abilities. Targeting the hyaluronan-CD44 pathway seems to have been bypassed by conventional mainstream oncological practice. There are existing drugs that decrease the activity/expression of hyaluronan and CD44: 4-methylumbelliferone and bromelain respectively. Some drugs inhibit hyaluronan-producing cells such as pirfenidone. The association of these three drugs has never been tested either in the laboratory or in the clinical setting. We present a hypothesis, sustained by hard experimental evidence, suggesting that the simultaneous use of these nontoxic drugs can achieve synergistic or added effects in reducing invasion and metastatic potential, in PDAC. A non-toxic, low-cost scheme for inhibiting this pathway may offer an additional weapon for treating pancreatic cancer.
胰腺导管腺癌 (PDAC) 是最致命的恶性肿瘤之一。目前的治疗方法并没有真正改善降低高死亡率和疾病的短生存期。5 年后的平均生存率低于 5%。需要新的创新疗法来扭转这种局面。非常密集的胰腺癌基质是一种障碍,它阻碍了化疗药物的进入,同时与肿瘤建立了一种促增殖的共生关系,因此许多作者都提出了靶向基质的方法。到目前为止,还没有发现针对这种靶向作用的理想药物或药物组合。考虑到这一目标,我们在这里根据大量关于重新利用药物的先前出版物,探索了一种不同的补充治疗方法。细胞表面蛋白 CD44 是透明质酸结合的主要受体。许多恶性肿瘤都表现出两者的过度表达/过度活跃。这在胰腺癌中尤为显著。已经发现抑制透明质酸产生细胞、透明质酸合成和/或 CD44 表达的独立抑制可降低肿瘤细胞的增殖、迁移、侵袭和转移能力。靶向透明质酸-CD44 途径似乎已被传统主流肿瘤学实践所绕过。有一些降低透明质酸和 CD44 活性/表达的现有药物:4-甲基伞形酮和菠萝蛋白酶分别。一些药物抑制透明质酸产生细胞,如吡非尼酮。这三种药物的联合从未在实验室或临床环境中进行过测试。我们提出了一个假设,该假设得到了坚实的实验证据的支持,即同时使用这些非毒性药物可以在减少 PDAC 的侵袭和转移潜力方面产生协同或附加作用。抑制这种途径的非毒性、低成本方案可能为治疗胰腺癌提供另一种手段。