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[俄罗斯抗肿瘤化合物氯尼索尔在眼睑肿瘤模型中的活性(实验研究)]

[Activity of the Russian antitumor compound chlonisol in models of eyelid tumors (experimental study)].

作者信息

Stukov A N, Kharitonova N N, Kulikov A N, Vershinina S F, Murazov Ya G, Zmitrichenko Yu G, Senchik K Yu, Tochilnikov G V, Ermakova E D, Filatova L V, Latipova D Kh, Semiglazova T Yu

机构信息

N.N. Petrov National Medical Research Center of Oncology, Saint Petersburg, Russia.

Military Medical Academy named after S.M. Kirov, Saint Petersburg, Russia.

出版信息

Vestn Oftalmol. 2022;138(4):6-14. doi: 10.17116/oftalma20221380416.

DOI:10.17116/oftalma20221380416
PMID:36004585
Abstract

UNLABELLED

Eyelid tumors are the most common neoplasms in everyday ophthalmic practice and cover a wide range of benign and malignant lesions. Surgical methods, cryodestruction, laser therapy and radiation therapy are used in the treatment of malignant eyelid tumors. Chemotherapy does not occupy a prominent place in the treatment of malignant eyelid tumors, its use is limited to sensitive tumors.

OBJECTIVE

To assess the antitumor activity of the Russian-developed chemical compound 2-[3-(2-chloroethyl)-3-nitrosoureido]-1.3-propandiol (chlonisol) on the models of transplantable tumors of various histogenesis implanted into the lower eyelid.

MATERIAL AND METHODS

The study was carried out on 67 mice of lines 129/SN, BALB/c and C57BL/6 that had Ehrlich carcinoma, sarcoma 37, lymphosarcoma LIO-1 and B16 melanoma transplanted into the eyelid. Tumor transplantation was done by injecting 0.05 ml of sterile sodium chloride solution containing 10 cells of Ehrlich carcinoma, sarcoma 37, lymphosarcoma LIO-1, or 10% suspension of tumor tissue of B16 melanoma. The injection was performed into the right lower eyelid in the direction from the outer towards the inner corner of the eye using a thin needle (29G). Chlonisol was administered at the maximum tolerated dose of 20 mg/kg or at the lower dose of 15 mg/kg intraperitoneally 24 hours after tumor transplantation.

RESULTS

In mice with Ehrlich carcinoma, sarcoma 37, lymphosarcoma LIO-1 and melanoma B16 transplanted under the skin of the lower eyelid, a single intraperitoneal injection of chlonisol at the dose of 20 or 15 mg/kg caused significant inhibition of tumor growth reaching 100%. Chlonisol significantly increased overall survival in animals with Ehrlich carcinoma (log rank test, =0.0464), sarcoma 37 (log rank test, <0.0001), lymphosarcoma LIO-1 (log rank test, =0.0122) and B16 melanoma (log rank test, <0.0001); the proportion of animals that were fully healed was 25, 78, 67 and 25%, respectively.

CONCLUSION

Chlonisol has a pronounced antitumor effect in mice with Ehrlich carcinoma, sarcoma 37, lymphosarcoma LIO-1 and B16 melanoma transplanted into the eyelid.

摘要

未标注

眼睑肿瘤是日常眼科实践中最常见的肿瘤,涵盖了广泛的良性和恶性病变。手术方法、冷冻治疗、激光治疗和放射治疗用于治疗恶性眼睑肿瘤。化疗在恶性眼睑肿瘤的治疗中并不占据突出地位,其应用仅限于敏感肿瘤。

目的

评估俄罗斯研发的化合物2-[3-(2-氯乙基)-3-亚硝基脲基]-1,3-丙二醇(氯尼索尔)对植入下眼睑的各种组织发生的可移植肿瘤模型的抗肿瘤活性。

材料与方法

研究在129/SN、BALB/c和C57BL/6品系的67只小鼠上进行,这些小鼠的下眼睑植入了艾氏癌、肉瘤37、淋巴肉瘤LIO-1和B16黑色素瘤。通过注射0.05 ml含有10个艾氏癌细胞、肉瘤37细胞、淋巴肉瘤LIO-1细胞的无菌氯化钠溶液或10%的B16黑色素瘤肿瘤组织悬液进行肿瘤移植。使用细针(29G)从眼外角向内角方向注射到右下眼睑。在肿瘤移植后24小时,以20 mg/kg的最大耐受剂量或15 mg/kg的较低剂量腹腔注射氯尼索尔。

结果

在右下眼睑皮下植入艾氏癌、肉瘤37、淋巴肉瘤LIO-1和黑色素瘤B16的小鼠中,单次腹腔注射20 mg/kg或15 mg/kg剂量的氯尼索尔可显著抑制肿瘤生长,抑制率达100%。氯尼索尔显著提高了艾氏癌(对数秩检验,P = 0.0464)、肉瘤37(对数秩检验,P < 0.0001)、淋巴肉瘤LIO-1(对数秩检验,P = 0.0122)和B16黑色素瘤(对数秩检验,P < 0.0001)动物的总生存率;完全治愈的动物比例分别为25%、78%、67%和25%。

结论

氯尼索尔对植入下眼睑的艾氏癌、肉瘤37、淋巴肉瘤LIO-1和B16黑色素瘤小鼠具有显著的抗肿瘤作用。

相似文献

1
[Activity of the Russian antitumor compound chlonisol in models of eyelid tumors (experimental study)].[俄罗斯抗肿瘤化合物氯尼索尔在眼睑肿瘤模型中的活性(实验研究)]
Vestn Oftalmol. 2022;138(4):6-14. doi: 10.17116/oftalma20221380416.
2
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Antibiot Khimioter. 1989 Feb;34(2):105-8.
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Gene transfer of a soluble receptor of VEGF inhibits the growth of experimental eyelid malignant melanoma.血管内皮生长因子可溶性受体的基因转移抑制实验性眼睑恶性黑色素瘤的生长。
Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2395-403.
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Int J Cancer. 1984 Aug 15;34(2):263-7. doi: 10.1002/ijc.2910340219.
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In vivo activity on murine tumors of a novel antitumor compound, N-beta-dimethylaminoethyl 9-carboxy-5-hydroxy-10-methoxybenzo[a]phenazine-6-carboxamide sodium salt (NC-190).新型抗肿瘤化合物N-β-二甲基氨基乙基9-羧基-5-羟基-10-甲氧基苯并[a]吩嗪-6-羧酰胺钠盐(NC-190)对小鼠肿瘤的体内活性
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