Cancer remains a significant global burden (
21-
24), (
25-
30), and the economic impact of COVID-19 has exacerbated the challenges faced in healthcare (
31-
37). This dual strain highlights the urgent need for innovative approaches in treating lung cancer. The present study investigates the interplay between the Wnt/β-catenin network and SIRT2 in lung cancer, revealing novel insights into their regulatory mechanisms and functional roles in cancer progression.
Our outcomes validate that activation of the Wnt/β-catenin cascade raises SIRT2 expression at both protein and mRNA levels in A549 lung cancer cell lines, while inhibition of this pathway reduces SIRT2 expression. This suggests that SIRT2 is a downstream target of Wnt/β-catenin, as further illustrated in Appendix 2 in Supplementary File. Supporting this, other studies have shown similar regulatory mechanisms; for instance, Chen et al. reported that Wnt/β-catenin signal transduction upregulates SIRT2 in hepatocellular carcinoma, enhancing tumor growth and metastasis (
36). This suggests that SIRT2 may serve as a key mediator of Wnt/β-catenin signaling in lung cancer, and similar mechanisms could apply to other cancers.
The study also explores the effects of RSV infection, which has been shown to modulate the Wnt/β-catenin pathway. The RSV infection alone led to a significant increase in SIRT2 expression, supporting the idea that RSV infection can enhance Wnt/β-catenin signaling. Moreover, when combined with Wnt3a, a Wnt agonist, RSV infection further augmented SIRT2 expression, indicating a synergistic effect. This enhancement underscores the potential for combining RSV and Wnt3a as therapeutic strategies to regulate SIRT2 expression in lung cancer.
One of the major findings of our study is that SIRT2 promotes lung cancer cell proliferation. This was evidenced by increased MTT assay absorbance and elevated cyclin D1 expression upon SIRT2 overexpression. Conversely, SIRT2 knockdown resulted in decreased cell proliferation and cyclin D1 levels. Our findings are consistent with those of Kim et al., who demonstrated that SIRT2 enhances cell cycle progression by regulating cyclin D1 expression in breast cancer (
37). Moreover, we observed a synergistic enhancement of oncogenic markers, such as cyclin D1 and c-Myc, when SIRT2 and Wnt/β-catenin were co-activated. This combined effect further highlights the role of SIRT2 in driving oncogenesis, consistent with Zhang et al., who reported that SIRT2 enhances Wnt/β-catenin signaling in colorectal cancer, contributing to tumor progression (
38).
Beyond its role in cell proliferation, our study also reveals that SIRT2 inhibits apoptosis in lung cancer cells. This is evident from the increased levels of cleaved caspase-3 and PARP following SIRT2 inhibition. However, SIRT2 overexpression diminished this apoptotic effect, suggesting that SIRT2 plays an anti-apoptotic role in lung cancer cells. This finding is consistent with previous studies showing that SIRT2 protects cancer cells, such as in pancreatic cancer, by deacetylating key apoptotic proteins (
39-
41). These results suggest that SIRT2 may not only promote cell survival and proliferation but also act as a potential target for therapeutic strategies aimed at inducing apoptosis in lung cancer.
Our study suggests that SIRT2 may play a central role in lung cancer progression by enhancing cell proliferation and inhibiting apoptosis. The dual regulation of SIRT2 by Wnt/β-catenin and RSV infection may create an oncogenic environment that fosters tumor growth. The upregulation of cyclin D1, Ki-67, and Bcl-2, along with downregulation of cleaved caspase-3 and PARP, suggests that SIRT2 may influence key cell cycle and apoptosis regulators, which are pivotal in cancer progression. These findings propose SIRT2 as a potential therapeutic target for lung cancer treatment, with its inhibition offering a route to promote tumor cell apoptosis and suppress proliferation.
The translational potential of our findings lies in identifying novel therapeutic strategies targeting SIRT2 in lung cancer. While our study offers promising insights, transitioning from laboratory findings to clinical applications requires further steps. First, the optimization of SIRT2 inhibitors and their integration with existing therapies must be explored in preclinical in vivo models. Such models could better simulate the tumor microenvironment (TME) and the effects of combination treatments, providing a clearer picture of their clinical viability. Additionally, exploring the use of RSV and Wnt3a as potential adjunct therapies in clinical settings may yield significant benefits, particularly in targeting specific oncogenic pathways like Wnt/β-catenin. Ultimately, clinical trials will be essential to evaluate the safety, efficacy, and pharmacokinetics of these strategies in diverse patient populations. These steps are crucial to bridging the gap between experimental models and real-world clinical applications, ultimately enhancing the therapeutic options available for lung cancer patients.
While this study offers valuable insights into the regulatory mechanisms governing SIRT2 in lung cancer, several areas require further investigation. One key limitation is the reliance on in vitro models using the A549 lung cancer cell line. Although these findings offer valuable mechanistic insights, validation in in vivo models or patient-derived tissues would be necessary to fully understand the clinical relevance of SIRT2 in lung cancer. Additionally, our study does not address potential variations in SIRT2 regulation across different lung cancer subtypes or patient demographics. Future research should explore how genetic, epigenetic, and environmental factors influence SIRT2 expression and its role in lung cancer progression.
Targeting SIRT2 for lung cancer therapy may pose challenges due to its involvement in various cellular processes, potentially leading to off-target effects in normal tissues. Developing tissue-specific inhibitors or delivery systems is essential to minimize these risks and ensure the safety of SIRT2-based therapies. Furthermore, identifying the specific transcription factors or co-regulators involved in β-catenin-mediated SIRT2 upregulation could enhance our understanding of this pathway and its therapeutic implications.
Additionally, our study does not fully consider the influence of the TME on SIRT2-mediated lung cancer progression. The TME consists of immune cells, fibroblasts, extracellular matrix components, and angiogenic factors that interact dynamically with tumor cells. Since our study utilized a 2D monolayer culture system, it does not completely capture these complex interactions. Future studies incorporating 3D spheroid models, co-culture systems with stromal and immune cells, or patient-derived xenografts (PDX) could provide a more physiologically relevant understanding of SIRT2’s role in lung cancer progression. Exploring how SIRT2 functions within an immune-rich microenvironment may further reveal its potential as a therapeutic target.
5.1. Conclusions
The present study underscores the critical role of the Wnt/β-catenin signaling pathway in regulating SIRT2 expression in lung cancer cells, demonstrating how RSV infection and Wnt3a activation synergistically enhance SIRT2 levels. Additionally, we provide evidence that SIRT2 promotes lung cancer cell proliferation while inhibiting apoptosis, suggesting that targeting SIRT2 may serve as a viable therapeutic approach for lung cancer treatment. However, further in vivo and clinical studies are necessary to validate these findings and determine the potential of SIRT2-targeted therapies in personalized medicine.