A novel role of LncRNA in regulating tumor metabolism and angiogenesis under hypoxia
triple-negative breast cancer
LncRNA for calcium-depended kinase activation
pregnancy up-regulated non-ubiquitously expressed calmodulin kinase
nuclear factor kappa-light-chain-enhancer of activated B cells
NF-kappa-B inhibitor alpha
inhibitor of nuclear factor kappa-B kinases
glucose transporter 3
vascular endothelial growth factor
inhibitor of nuclear factor kappa-B kinase subunit beta
Tumor cells are characterized by metabolic reprogramming, a step that is necessary to support their high demand for energy and nutrients [1, 2]. Furthermore, once metastatic tumor cells are seeded, tumor microenvironment remodeling is immediately initiated, leading to the formation of more suitable conditions for growth. Tumor cells secrete several types of growth factors, cytokines, and chemokines to induce angiogenesis and tumor-associated immune cell recruitment, all of which can promote proliferation and metastasis, as well as trigger immune tolerance and drug resistance . Exploring the synergistic effect between metabolic reprogramming and microenvironment remodeling will likely facilitate the discovery of novel biomarkers and therapeutic targets.
Calcium is an important second messenger in cell signaling modulation. Normally, intracellular calcium performs its signaling functions by activating the calmodulin (CaM) and CaM kinases (CaMKs). The latest research has conclusively demonstrated that calcium flux plays a critical role in tumor progression , although how this flux mediates the interconnections between calcium signaling and other pathways is unclear.
Breast cancer is the most common malignancy and the leading cause of cancer death among women worldwide . For this reason, the development of more efficient therapeutic strategies and targets is urgently needed, especially for patients with triple-negative breast cancer (TNBC). A deeper understanding of breast cancer pathogenesis may accelerate the development of therapeutic strategies and targets and thereby improve the outcomes of TNBC patients.
RNA pull-down followed by mass spectrometry analysis revealed that CamK-A was a binding partner of pregnancy-up-regulated, non-ubiquitously expressed CaMK (PNCK) and NF-kappa-B inhibitor alpha (IκBα). Using an in vitro kinase assay, the authors demonstrated that CamK-A facilitated PNCK activation, enabling the kinase to phosphorylate IκBα at Ser32 and ultimately triggering calcium-induced NF-kB signaling activity. In support of this result, a pathway reporter array confirmed that the NF-κB pathway was regulated by CamK-A. Thus, the authors described a model in which CamK-A promoted PNCK self-activation, IκBα phosphorylation, and subsequent activation of the NF-κB signaling pathway.
Sang et al. also identified an important link between hypoxia and calcium signaling. Specifically, hypoxia can induce cellular reactive oxygen species production and endoplasmic reticulum stress, leading to increased cytosolic calcium levels. This process is thought to be a crucial microenvironmental element for stimulating solid tumor growth, but the details have remained elusive. Sang et al. demonstrated that by increasing tumor cytosolic calcium concentrations, hypoxia could activate the PNCK-CamK-A-NF-κB axis and its downstream target genes, including glucose transporter 3 (GLUT3), interleukin 6 (IL-6), interleukin 8 (IL-8), and vascular endothelial growth factor (VEGF). This mechanism induces uncontrolled glucose uptake, tumor-associated macrophage recruitment, intra-tumoral angiogenesis, and tumor microenvironment remodeling.
It is widely assumed that inhibitor of nuclear factor kappa-B kinases (IKKs) phosphorylate IκBα to activate the NF-κB pathway. Therefore, CaMKs are believed to regulate NF-κB through IKKs. However, this study demonstrated that neither knockout nor knockdown of IKK subunit beta (IKKβ) had any effect on PNCK-CamK-A axis-mediated IκBα phosphorylation. This finding indicates that CaMKs can activate the NF-κB pathway in an IKK-independent manner, providing a major advance in our understanding of calcium-dependent NF-κB pathway activation.
As clinical specimen analysis revealed both that CamK-A was highly expressed in tumor tissues versus adjacent normal tissues and that its high expression was associated with poor clinical outcomes of patients with breast cancer, Sang et al. examined the role of CamK-A in tumorigenesis using a patient-derived xenograft model (PDX) of TNBC. In this system, the suppression of CamK-A using in vivo-optimized RNAi led to robust suppression of tumor proliferation, microvascular tumor growth, macrophage recruitment, and, thereby, tumor microenvironment remodeling. These strong data pave the way for the further clinical application of CamK-A inhibition. Excitingly, the novel RNAi-based drug, Patisiran (ONPATTOR™) has recently been approved by the US Food and Drug Administration , and many more RNAi drugs will likely be developed in the coming years. LncRNA-targeting drugs may contribute to the emergence of RNAi drugs given the tissue specificity of these macromolecules. Exploring CamK-A’s therapeutic possibilities would be an exciting step along this path.
In summary, the lncRNA CamK-A activates the calcium signaling pathway under hypoxic tumor conditions, in turn inducing the activation of the CaMK-dependent NF-κB pathway and tumor microenvironment remodeling. Additionally, CamK-A plays a key role in tumor development, and interference of this lncRNA can robustly block cancer progress, highlighting its potential role in anti-cancer therapy.
JL and JL wrote the manuscript with the help of LFL. The manuscript was edited by JL and LFL in their private capacity. No official support or endorsement by the National Institutes of Health, National Institute of Environmental Health is intended or should be inferred. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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