Editorial: Tumor-host interactions: metabolic and signaling pathways altered in cancer, immune and stromal cells

Tumor-host interactions within the tumor microenvironment (TME) represent a critical area of cancer research. The TME is characterized by hypoxia, nutrient competition, acidic pH, chronic inflammation, and dynamic communication between cancer, immune, and stromal cells. These interactions involve the release of soluble factors such as metabolites, cytokines, growth factors, and exosomes, which drive aberrant signaling pathways and phenotypic and metabolic plasticity in both tumor and immune cells (De Visser K.E., et al, 2023) This metabolic adaptation is crucial for tumor growth, metastatic dissemination, and therapy resistance. Recent studies have highlighted the potential of targeting altered signaling and tumor metabolism as a promising approach for the development of new cancer therapies (Bejarano L., et al, 2021;Dominiak A., et al, 2020) Together, these findings suggest that curcumin could be considered a promising candidate for OSCC therapy, a cancer type that is often refractory to current treatment strategies. In the brief research paper by Du et al., the authors explored the role of Krüppel-like factor 14 (KLF14) and its underlying mechanism(s) of action in cell-cycle regulation in cervical cancer. KLF14, a member of the Krüppel-like transcription factor family (KLFs), acts as a key regulator of tumor pathogenesis. Throught a lentivirus infection leading to stable overexpression of KLF14 the authors identified that this factor induces S-phase arrest in cervical cancer cells and inhibited the proliferation of cervical cancer cells in vivo. The induction of S-phase arrest was related to its zinc-finger structure. Moreover, KLF14 also activates the JNK pathway to induce S-phase arrest and promote the expression of cyclindependent kinase 2 (CDK2) and cyclin A2 (CCNA2). Therefore, this study opened the way for future investigation on KLF14 manipulation for cancer therapy. Lastly, the review paper by Hernández-Magaña et al., addressed the emergence of rationally designed cancer therapies that target cell plasticity mechanisms, particularly those involved in epithelialmesenchymal transition (EMT). These strategies aim to block the transformation of epithelial cells into cancerous phenotypes. The authors focused on hepatocellular carcinoma (HCC) and reviewed engineering principles that could be applied to the rational design of personalized therapeutic approaches. They described multiple HCC features associated with phenotypic plasticity across different biological levels and supported the development of models that accurately represent EMT dynamics. The conceptualization of such models may enable the application of engineering principles to design and optimize cancer treatments, highlighting emerging research areas such as systems biology.In conclusion, the studies collected in this Research Topic underscore the pivotal role of metabolic and signaling plasticity in tumor-host interactions within the TME. By combining computational, experimental, and conceptual approaches, these studies provide complementary insights into how hypoxia, metabolic rewiring, cell-cycle regulation, and phenotypic plasticity drive cancer progression and therapeutic resistance. Together, they highlight the importance of integrative and interdisciplinary strategies to better understand TME complexity and to advance the development of more effective and personalized anticancer therapies.