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口服乳铁蛋白可抑制已形成肿瘤的生长,并增强传统化疗效果。

Oral lactoferrin inhibits growth of established tumors and potentiates conventional chemotherapy.

作者信息

Varadhachary Atul, Wolf Jeffrey S, Petrak Karel, O'Malley Bert W, Spadaro Michela, Curcio Claudia, Forni Guido, Pericle Federica

机构信息

Agennix, Inc., Houston, TX 77046, USA.

出版信息

Int J Cancer. 2004 Sep 1;111(3):398-403. doi: 10.1002/ijc.20271.

Abstract

In this work, we investigated the anticancer activity of orally administered recombinant human lactoferrin (rhLF) alone and in combination with chemotherapy in tumor-bearing mice. rhLF inhibited the growth of squamous cell carcinoma (O12) tumors in T cell-immunocompromised nu/nu mice by 80% when administered at 1,000 mg/kg (2.9 g/m2) by oral gavage twice daily for 8 days (p < 0.001). Similar activity was observed in syngeneic, immunocompetent BALB/c mice, where orally administered rhLF (1,000 mg/kg, 2.9 g/m2 once daily) halted the growth of mammary adenocarcinoma TUBO. Oral rhLF (200 mg/kg, 0.57 g/m2) was also used alone and in combination with cis-platinum (5 mg/kg) to treat head-and-neck squamous cell carcinoma in a syngeneic murine model. Monotherapy with oral rhLF or cis-platinum caused 61% or 66% tumor growth inhibition over placebo, respectively. Mice receiving both therapies showed 79% growth inhibition, a statistically significant improvement over each drug alone. We then demonstrated that administration of oral rhLF (300 mg/kg, 0.86 g/m2) to tumor-bearing or naive mice resulted in (i) significantly increased production of IL-18 in the intestinal tract, (ii) systemic NK cell activation and (iii) circulating CD8+ T-cell expansion. These data suggest that oral rhLF is an immunomodulatory agent active against cancer as a single agent and in combination chemotherapy, exerting its systemic effect through stimulation of IL-18 and other cytokines in the gut enterocytes. rhLF has been administered orally to 211 people without a single serious drug-related adverse event. Thus, rhLF shows promise as a safe and well-tolerated novel immunomodulatory anticancer agent.

摘要

在本研究中,我们调查了口服重组人乳铁蛋白(rhLF)单独及与化疗联合应用对荷瘤小鼠的抗癌活性。当以1000mg/kg(2.9g/m²)的剂量通过口服灌胃,每天两次,连续8天给药时,rhLF可使T细胞免疫缺陷的裸鼠(nu/nu)体内的鳞状细胞癌(O12)肿瘤生长抑制80%(p<0.001)。在同基因、具有免疫活性的BALB/c小鼠中也观察到了类似的活性,口服rhLF(1000mg/kg,2.9g/m²,每天一次)可使乳腺腺癌TUBO的生长停止。口服rhLF(200mg/kg,0.57g/m²)也单独或与顺铂(5mg/kg)联合用于同基因小鼠模型中治疗头颈部鳞状细胞癌。口服rhLF或顺铂单药治疗相对于安慰剂分别导致61%或66%的肿瘤生长抑制。接受两种治疗的小鼠显示出79%的生长抑制,相对于每种药物单独使用有统计学上的显著改善。然后我们证明,给荷瘤或未荷瘤小鼠口服rhLF(300mg/kg,0.86g/m²)会导致:(i)肠道中IL-18的产生显著增加;(ii)全身自然杀伤细胞活化;(iii)循环CD8⁺T细胞扩增。这些数据表明,口服rhLF作为单一药物和联合化疗时都是一种对癌症有效的免疫调节剂,通过刺激肠道肠细胞中的IL-18和其他细胞因子发挥其全身作用。rhLF已口服给药于211人,未发生一例严重的药物相关不良事件。因此,rhLF有望成为一种安全且耐受性良好的新型免疫调节抗癌药物。

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