Wake Forest Department of General Surgery, Wake Forest Organoid Research Center (WFORCE), Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Wake Forest Institute of Regenerative Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Ann Surg Oncol. 2024 Aug;31(8):5377-5389. doi: 10.1245/s10434-024-15355-0. Epub 2024 May 4.
Appendiceal cancer (AC) excessive mucin production is a barrier to heated intraperitoneal chemotherapy (HIPEC) drug delivery. Bromelain is a pineapple stem extract with mucolytic properties. We explored bromelain treatment effects against mucinous AC in a patient-derived tumor organoid (PTO) model and an AC cell line.
PTOs were fabricated from tumor specimens obtained from patients with AC undergoing cytoreductive surgery with HIPEC. PTOs underwent HIPEC treatment with bromelain, cisplatin, and mitomycin C (MMC) at 37 °C and 42 °C with and without bromelain pretreatment.
From October 2020 to May 2023, 16 specimens were collected from 13 patients with low-grade (12/16, 75%) and high-grade AC (4/16, 25%). The mucin-depleting effects of bromelain were most significant in combination with N-acetylcysteine (NAC) compared with bromelain (47% versus 10%, p = 0.0009) or NAC alone (47% versus 12.8%, p = 0.0027). Bromelain demonstrated > 31% organoid viability reduction at 60 min (p < 0.001) and > 66% in 48 h (p < 0.0001). Pretreatment with bromelain increased cytotoxicity of both cisplatin and MMC HIPEC conditions by 31.6% (p = 0.0001) and 35.5% (p = 0.0001), respectively. Ki67, CK20, and MUC2 expression decreased after bromelain treatment; while increased caspase 3/7 activity and decreased Bcl-2 (p = 0.009) and Bcl-xL (p = 0.01) suggest induction of apoptosis pathways. Furthermore, autophagy proteins LC3A/B I (p < 0.03) and II (p < 0.031) were increased; while ATG7 (p < 0.01), ATG 12 (p < 0.04), and Becline 1(p < 0.03), expression decreased in bromelain-treated PTOs.
Bromelain demonstrates cytotoxicity and mucolytic activity against appendiceal cancer organoids. As a pretreatment agent, it potentiates the cytotoxicity of multiple HIPEC regimens, potentially mediated through programmed cell death and autophagy.
阑尾癌(AC)过度产生粘蛋白是阻碍腹腔内热化疗(HIPEC)药物输送的一个障碍。菠萝蛋白酶是一种具有粘液溶解特性的菠萝茎提取物。我们在患者来源的肿瘤类器官(PTO)模型和阑尾癌细胞系中探索了菠萝蛋白酶治疗粘蛋白性 AC 的效果。
从接受细胞减灭术联合 HIPEC 的 AC 患者的肿瘤标本中制备 PTO。PTO 在 37°C 和 42°C 下用菠萝蛋白酶、顺铂和丝裂霉素 C(MMC)进行 HIPEC 治疗,并在进行 HIPEC 治疗之前用菠萝蛋白酶预处理。
从 2020 年 10 月至 2023 年 5 月,从 13 名接受低级别(12/16,75%)和高级别(4/16,25%)AC 手术的患者中收集了 16 个标本。与单独使用菠萝蛋白酶(47%对 10%,p=0.0009)或单独使用 N-乙酰半胱氨酸(NAC)(47%对 12.8%,p=0.0027)相比,菠萝蛋白酶联合 NAC 的粘液消耗作用最为显著。菠萝蛋白酶在 60 分钟时使类器官活力降低超过 31%(p<0.001),在 48 小时时降低超过 66%(p<0.0001)。菠萝蛋白酶预处理分别使顺铂和 MMC HIPEC 条件下的细胞毒性增加 31.6%(p=0.0001)和 35.5%(p=0.0001)。菠萝蛋白酶处理后 Ki67、CK20 和 MUC2 的表达减少,而 caspase 3/7 活性增加,Bcl-2(p=0.009)和 Bcl-xL(p=0.01)减少,提示诱导细胞凋亡途径。此外,自噬蛋白 LC3A/B I(p<0.03)和 II(p<0.031)增加,而 ATG7(p<0.01)、ATG 12(p<0.04)和 Becline 1(p<0.03)表达减少。
菠萝蛋白酶对阑尾癌类器官具有细胞毒性和粘液溶解活性。作为预处理剂,它增强了多种 HIPEC 方案的细胞毒性,可能通过程序性细胞死亡和自噬介导。