Suppr超能文献

保持端粒短!一种创新的肿瘤内长期药物输送系统。

Keeping those telomeres short! an innovative intratumoral long-term drug delivery system.

机构信息

Jerry J. Cohen Radiobiology Research Laboratory, Ben Gurion University, 84105, Beer Sheva, Israel,

出版信息

J Cancer Res Clin Oncol. 2015 Jan;141(1):23-34. doi: 10.1007/s00432-014-1747-7. Epub 2014 Jul 30.

Abstract

BACKGROUND

Telomerase activation and an alternative lengthening of telomeres (ALT) mechanism are two telomere-lengthening cancer cell survival mechanisms elicited by both chemo- and/or radiotherapy. Telomere lengthening interferes with cell lethality and results in the immortalization of cancer cells. To counteract these mechanisms, we developed a drug delivery system (DDS) consisting of a polymeric implant that is inserted directly into tumors. The DDS releases, continuously and gradually, a cationic porphyrin (PdTMPyP4) for >30 days after a single application, and inhibits telomerase activation.

METHODS

The PdTMPyP4 porphyrin is incorporated into a poly(co-glycolic lactic)acid (PLGA) polymer, solidified and cut into small rods. PdTMPyP4 release from the rods was measured spectrophotometrically over time. Uptake of Pd in the DNA of in L428 Hodgkins lymphoma cells was measured by ICP-MS, and telomerase activation by the TRAP assay. The rods were placed into the growth medium of cells whose growth rate was measured for 11 and 19 days. The cylinders were also inserted directly into KHJJ murine mammary tumors borne on the thighs of BALB/c mice and the tumor growth rate measured.

RESULTS

In vitro, >10(9)Pd atoms were measured in the DNA of each L428 cell and telomerase activity was reduced by ~15% within 24 h. A one-time application of the rod in the cell medium induced a factor of >5 greater lethality compared to a blank rod or untreated controls. In vivo, a one-time insertion of the rod into tumors resulted in the retardation of the growth rate by factors of 3-5 compared to untreated controls. Systemic uptake after intratumoral insertion of the rod was negligible.

CONCLUSION

The results suggest that the direct intratumoral insertion of a PdTMPyP4-containing polymeric rod would be of benefit as an adjuvant treatment for patients undergoing chemo- or radiotherapy. By preventing the lengthening of telomeres and therefore the unrestricted growth of cancer cells, our DDS will provide a significant therapeutic advantage to these treatments without affecting normal tissues.

摘要

背景

端粒酶激活和端粒的替代性延长(ALT)机制是化学疗法和/或放射疗法引起的两种延长端粒的癌细胞存活机制。端粒的延长会干扰细胞致死性,并导致癌细胞的永生。为了对抗这些机制,我们开发了一种药物输送系统(DDS),该系统由直接插入肿瘤的聚合物植入物组成。DDS 在单次应用后持续且逐渐释放出阳离子卟啉(PdTMPyP4),持续超过 30 天,并抑制端粒酶激活。

方法

将 PdTMPyP4 卟啉掺入聚(共-乙交酯乳酸)(PLGA)聚合物中,固化并切成小棒。通过分光光度法随时间测量棒从 PdTMPyP4 的释放。通过 ICP-MS 测量 L428 霍奇金淋巴瘤细胞中 DNA 中 Pd 的摄取,并通过 TRAP 测定法测量端粒酶激活。将棒放入细胞生长培养基中,测量其 11 天和 19 天的生长速度。还将圆柱体直接插入大腿上带有 KHJJ 鼠乳腺肿瘤的 BALB/c 小鼠的肿瘤中,并测量肿瘤生长速度。

结果

在体外,每个 L428 细胞的 DNA 中测量到超过 10(9)Pd 原子,并且在 24 小时内端粒酶活性降低了约 15%。在细胞培养基中一次性应用棒比空白棒或未经处理的对照诱导更高的致死率因子> 5。在体内,与未经处理的对照相比,将棒一次性插入肿瘤中会导致肿瘤生长速度减慢 3-5 倍。瘤内插入棒后的全身摄取可以忽略不计。

结论

结果表明,将含 PdTMPyP4 的聚合物棒直接插入肿瘤中作为化学疗法或放射疗法患者的辅助治疗将是有益的。通过防止端粒的延长,从而防止癌细胞的无限制生长,我们的 DDS 将为这些治疗方法提供重要的治疗优势,而不会影响正常组织。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验