Taizhou Municipal Hospital - Department of Pathology - Zhejiang Province, Taizhou Zhejiang, China.
The 940th Hospital of Joint Logistics Support Force of PLA - Department of Mammary Gland - Lanzhou, Gansu, China.
Acta Cir Bras. 2024 May 24;39:e391624. doi: 10.1590/acb391624. eCollection 2024.
To evaluate the chemotherapeutic activity of temozolomide counter to mammary carcinoma.
In-vitro anticancer activity has been conducted on MCF7 cells, and mammary carcinoma has been induced in Wistar rats by introduction of 7, 12-Dimethylbenz(a)anthracene (DMBA), which was sustained for 24 weeks. Histopathology, immunohistochemistry, cell proliferation study and apoptosis assay via TUNEL method was conducted to evaluate an antineoplastic activity of temozolomide in rat breast tissue.
IC50 value of temozolomide in MCF7 cell has been obtained as 103 μM, which demonstrated an initiation of apoptosis. The temozolomide treatment facilitated cell cycle arrest in G2/M and S phase dose dependently. The treatment with temozolomide suggested decrease of the hyperplastic abrasions and renovation of the typical histological features of mammary tissue. Moreover, temozolomide therapy caused the downregulation of epidermal growth factor receptor, extracellular signal-regulated kinase, and metalloproteinase-1 expression and upstream of p53 and caspase-3 proliferation to indicate an initiation of apoptotic events.
The occurrence of mammary carcinoma has been significantly decreased by activation of apoptotic pathway and abrogation of cellular propagation that allowable for developing a suitable mechanistic pathway of temozolomide in order to facilitate chemotherapeutic approach.
评估替莫唑胺对乳腺癌的化疗活性。
在 MCF7 细胞上进行了体外抗癌活性研究,并通过引入 7,12-二甲基苯并(a)蒽(DMBA)在 Wistar 大鼠中诱导乳腺癌,持续 24 周。通过 TUNEL 法进行组织病理学、免疫组织化学、细胞增殖研究和细胞凋亡分析,以评估替莫唑胺在大鼠乳腺组织中的抗肿瘤活性。
替莫唑胺在 MCF7 细胞中的 IC50 值为 103μM,表明开始凋亡。替莫唑胺治疗可使细胞周期在 G2/M 和 S 期依赖性地停滞。替莫唑胺治疗可减少过度增生的磨损并恢复乳腺组织的典型组织学特征。此外,替莫唑胺治疗导致表皮生长因子受体、细胞外信号调节激酶和金属蛋白酶-1 的表达下调,以及 p53 和 caspase-3 增殖的上游下调,表明凋亡事件的开始。
通过激活凋亡途径和阻断细胞增殖,显著降低了乳腺癌的发生,为开发替莫唑胺的合适机制途径以促进化疗方法提供了可能。