Molecular Biomedicine Laboratory, Postgraduate Department of Studies and Research in Biotechnology, Sahyadri Science College, Kuvempu University, Shivamogga, 577203, Karnataka, India.
Molecular Biomedicine Laboratory, Postgraduate Department of Studies and Research in Biotechnology, Sahyadri Science College, Kuvempu University, Shivamogga, 577203, Karnataka, India; Division for DNA Repair Research, Department of Neurosurgery, Centre for Neuroregeneration, Houston Methodist, Fannin Street, Houston, TX, USA.
Phytomedicine. 2023 Oct;119:154981. doi: 10.1016/j.phymed.2023.154981. Epub 2023 Jul 18.
The declined oxygen tension in the cancer cell leads to the hypoxic adaptive response and favors establishment of tumor micro environment [TEM]. The complex TME consists of interwoven hypoxic HIF-1α and DNA damage repair ATM signaling. The ATM/HIF-1α phosphorylation switch on angiogenesis and abort apoptosis. Targeting this signaling nexus would be a novel therapeutic strategy for the treatment of cancer.
Steroidal alkaloid solanidine is known for varied pharmacological role but with less molecular evidences. Our earlier findings on solanidine proven its anti-neoplastic activity by inducing apoptosis in lung cancer. In continued research, efforts have been made to establish the underlying molecular signaling in induction of DNA damage in prevailing hypoxic TME.
The solanidine induced DNA damage was assessed trough alkali COMET assay; signaling nexus and gene expression profile analysis through IB, qRT-PCR, Gelatin Zymography, IHC, IF and ELISA. Pathophysiological modulations assessed through tube formation, migration, invasion assays. Anti-angiogenic studies through CAM, rat aorta, matrigel assays and corneal neovascularization assay. Anti-tumor activity through in-vivo DLA ascites tumor model and LLC model.
The results postulates, inhibition of hypoxia driven DDR proteins pATM/pHIF-1α by solanidine induces anti-angiogenesis. Systematic study of both non-tumorigenic and tumorigenic models in-vitro as well as in-vivo experimental system revealed the angio-regression mediated anticancer effect in lung cancer. These effects are due to the impeded expression of angiogenic mediators such as VEGF, MMP2&9 and inflammatory cytokines IL6 and TNFα to induce pathophysiological changes CONCLUSION: The study establishes new role of solanidine by targeting ATM/HIF-1α signaling to induce anti-angiogenesis for the first time. The study highlights the potentiality of plant based phytomedicine solanidine which can targets the multiple hallmarks of cancer by targeting interwoven signaling crosstalk. Such an approach through solanidine necessary to counteract heterogeneous complexity of cancer which could be nearly translated into drug.
癌细胞中氧气张力的下降导致缺氧适应性反应,并有利于肿瘤微环境 [TEM] 的建立。复杂的 TME 由交织的缺氧 HIF-1α 和 DNA 损伤修复 ATM 信号组成。ATM/HIF-1α 磷酸化开关促进血管生成并阻止细胞凋亡。针对这种信号连接将是治疗癌症的一种新的治疗策略。
甾体生物碱茄啶以多种药理作用而闻名,但分子证据较少。我们之前的研究表明,茄啶通过诱导肺癌细胞凋亡发挥其抗肿瘤活性。在继续的研究中,努力确定在流行的缺氧 TME 中诱导 DNA 损伤的潜在分子信号。
通过碱 COMET 测定评估茄啶诱导的 DNA 损伤;通过 IB、qRT-PCR、凝胶酶谱、IHC、IF 和 ELISA 分析信号连接和基因表达谱。通过管形成、迁移、侵袭测定评估病理生理调节。通过 CAM、大鼠主动脉、Matrigel 测定和角膜新生血管形成测定进行抗血管生成研究。通过体内 DLA 腹水肿瘤模型和 LLC 模型进行抗肿瘤活性研究。
结果表明,茄啶抑制缺氧驱动的 DDR 蛋白 pATM/pHIF-1α 诱导抗血管生成。在体外和体内实验系统中对非致瘤性和致瘤性模型进行系统研究,揭示了肺癌中的血管生成消退介导的抗癌作用。这些作用是由于血管生成介质如 VEGF、MMP2 和 9 和炎症细胞因子 IL6 和 TNFα 的表达受阻,导致病理生理变化。
该研究首次通过靶向 ATM/HIF-1α 信号来诱导抗血管生成,确立了茄啶的新作用。该研究强调了基于植物的植物药茄啶的潜力,它可以通过靶向交织的信号串扰来靶向癌症的多个标志。通过茄啶采取这种方法对于对抗癌症的异质性复杂性是必要的,这几乎可以转化为药物。