YAP-dependent metabolic remodeling in local lymph node boosts the function of cancer cells
Editorial Commentary

YAP-dependent metabolic remodeling in local lymph node boosts the function of cancer cells

Toshihide Kashihara, Daniela Zablocki, Junichi Sadoshima

Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, NJ, USA

Correspondence to: Junichi Sadoshima, MD, PhD. Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, 185 S. Orange Ave., MSB G609, Newark, NJ 07103, USA. Email: sadoshju@njms.rutgers.edu.

Provenance: This is an invited article commissioned by Executive Editor-in-Chief Dr. Hualin Sun (Jiangsu Key Laboratory of Neuroregeneration, Nantong University, Nantong, China).

Comment on: Lee CK, Jeong SH, Jang C, et al. Tumor metastasis to lymph nodes requires YAP-dependent metabolic adaptation. Science 2019;363:644-9.


Received: 26 July 2019; Accepted: 02 August 2019; Published: 23 August 2019.

doi: 10.21037/biotarget.2019.08.01


Cancer cells are remarkably flexible in their ability to adapt to various local environments to promote their survival, growth and invasion. A recent study by Koh’s laboratory suggests that metastatic cancer cells upregulate fatty acid oxidation (FAO) through activation of yes-associated protein (YAP), a major effector of the Hippo pathway, at local lymph nodes (LNs), which boosts the ability of the cancer cells to invade distant organs (1). We here discuss how YAP mediates the metabolic flexibility in metastatic cancer cells.

Cancer metastasis to the regional sentinel LNs, the most common site of metastasis of epithelial tumors, is one of the most important prognostic indicators for additional metastasis to other organs and mortality in cancer patients (2). Currently, there is no effective strategy for selectively targeting metastasis. Thus, a deeper understanding of the molecular mechanisms of the metastatic processes is essential.

Cancer cells initiate metastasis by entering the bloodstream, either directly or through the lymphatic system, and extravasate the bloodstream to land in foreign tissues, which provide a ‘congenial soil’ (the metastatic microenvironment) for ‘seeds’ (cancer cells) (3). They then begin to colonize ‘the congenial soil’, which supports cancer cell survival and outgrowth, accompanied by metabolic adaptation. However, how metastatic cancer cells survive and proliferate in the LNs remains poorly understood. In their recent publication, Lee et al. addressed this question and discovered that tumor cells that metastasize to LNs require YAP-dependent metabolic reprogramming to adapt to the new microenvironment (1).

Cancer cells have unique metabolic features (4). In general, non-cancer cells critically rely on mitochondrial oxidative phosphorylation of reducing equivalents derived from various energy sources, including lipids, glucose, amino acids, and ketone bodies, to generate ATP. On the other hand, cancer cells preferentially utilize cytosolic glycolysis to generate ATP, to provide cells with the intermediates needed for biosynthetic pathways, even under normoxic conditions, termed aerobic glycolysis or the Warburg effect (5). In addition, cancer cells have remarkable flexibility to strategically undergo metabolic reprogramming during the course of development in order to maintain bioenergetics and biosynthesis, according to the microenvironment in which they reside and the availability of nutrients therein (6). The ability of cancer cells to modulate their metabolism appears to be of particular importance during metastasis, allowing them to adapt to new environments. Increasing lines of evidence suggest that metastatic cancer cells and invasive cancer cells upregulate FAO to support their proliferative capacity (7). Currently, however, the signaling mechanisms through which metastatic cancer cells undergo metabolic remodeling are poorly understood.

Using comparative transcriptomics and metabolomics analysis, Lee et al. demonstrated that B16F10 melanoma cells from micrometastatic and macrometastatic tumor-draining LNs exhibit significant alterations in lipid metabolism, such as bile acid metabolism, fatty acid metabolism, cholesterol homeostasis, and oxidative phosphorylation, and that there is a greater accumulation of fatty acids in LN metastasized tumors than in primary tumors (1). Moreover, the LN metastasized tumors preferentially rely on FAO over glucose or glutamine oxidation as the major mechanism by which ATP is generated. Administration of etomoxir, an inhibitor of FAO, markedly suppressed LN metastasis without affecting primary tumor or tumor-draining LN size, or blood-borne metastasis to the lungs. These findings indicate that a metabolic shift to FAO is essential for metastatic tumors to survive and expand in the LNs. Although the authors do not provide mechanistic insights into how FAO contributes to LN metastasis, abundant production of ATP through FAO may be advantageous for cell proliferation, motility and invasion, key functions of metastatic cancer cells. For example, downstream metabolic intermediates and signaling mechanisms of FAO may affect survival and death through anoikis (8), as well as cell fate, such as epithelial mesenchymal transformation (9).

This raises the important question of how this metabolic remodeling is achieved in LNs. In this study, the authors showed that YAP, which is a major downstream effector of the Hippo signaling pathway, is activated in the cancer cells at the invasive front of LN-metastatic tumors, but not in primary tumors. Furthermore, knockdown of YAP attenuated FAO in LN-metastatic tumors without affecting glucose or glutamine oxidation (1). The authors also showed that YAP deletion markedly inhibited LN metastasis without changing the size of the primary tumor or LN, consistent with the effect of inhibition of FAO on LN metastasis. These results suggest that YAP promotes LN metastatic tumors through upregulation of FAO (Figure 1).

Figure 1 The molecular mechanism by which YAP mediates metabolic remodeling and growth of metastatic cancer cells in local lymph nodes. The microenvironment in local lymph nodes, such as the availability of fatty acids, promotes YAP-induced activation of fatty acid oxidation, which in turn boosts growth and invasiveness in metastatic cancer cells. Increased production of bile acids in lymph node-metastatic cancer cells activates YAP through unknown mechanisms. YAP activates fatty acid oxidation through interaction with unknown transcription factors. Interventions to inhibit bile acid synthesis, YAP or fatty acid oxidation may attenuate metastasis of cancer cells. YAP, yes-associated protein.

The Hippo signaling pathway is an evolutionarily conserved signaling pathway that regulates organ size and tumorigenesis (10). YAP and transcriptional coactivator with PDZ-binding motif (TAZ) are the two major terminal effectors, with partially overlapping functions, in the Hippo signaling pathway. YAP plays a crucial role in tissue homeostasis through regulation of proliferation, survival, and metabolism (10). When the Hippo signaling pathway is activated, the core kinase cascade phosphorylates YAP, thereby leading to cytosolic retention and inhibition of YAP. On the other hand, when the Hippo signaling pathway is inactivated, YAP is translocated to the nucleus and interacts with transcription factors to affect downstream target genes. The upstream components of the Hippo pathway act as tumor suppressors, whereas YAP/TAZ are often upregulated in cancer cells (11).

Lee et al. elegantly demonstrated that cancer cells activate YAP after they arrive at LNs, in response to the local environment (1). Both metabolomic and transcriptomic analyses revealed that bile acids are markedly elevated in LN-metastatic tumors. The authors confirmed that bile acids activate YAP in the LN-metastatic tumors and found that nuclear vitamin D receptor (VDR), one of the bile acid-activated receptors, likely mediates bile acid-induced YAP activation. It should be noted, however, that what triggers bile acid production in LN-metastatic tumors remains to be elucidated. Furthermore, in human hepatocytes, the VDR-signaling pathway acts as a negative feedback mechanism to suppress bile acid synthesis through downregulation of CYP7A1 (12). Thus, it would be interesting to investigate whether bile acid synthesis in the LN-metastatic tumors is sustainable. Although previous studies have shown that bile acids activate YAP through activation of either sphingosine 1-phosphate receptor 2 (13) or induction of IQGAP1, a scaffold protein (14), how the bile acids-VDR pathway affects the Hippo pathway and YAP in local LNs remains to be clarified.

Regardless of the open questions, perhaps one of the most crucial discoveries in the work by Lee et al. is that YAP confers metabolic flexibility to metastatic cancer cells. What, then, is the underlying mechanism through which YAP mediates the metabolic reprogramming in metastatic cancer cells? Because YAP is a transcriptional cofactor that lacks DNA-binding activity, it regulates gene expression through interaction with transcription factors. The TEAD family transcription factors are among the best characterized transcription factors mediating the function of YAP/TAZ through expression of genes promoting cell survival, proliferation, and metabolism (10). Interaction between YAP and TEADs may be involved in the regulation of tumor metastasis to LNs since the TEAD-interaction domain of YAP is essential for YAP-mediated tumor growth and metastasis in mammary carcinoma and melanoma (15). However, since YAP mediates the Warburg effect in primary cancer cells, it remains to be determined how YAP can mediate glycolysis under some conditions but stimulate FAO under other conditions. Although these metabolic conditions are not necessarily mutually exclusive, it appears that YAP selectively modulates FAO in metastatic cancer cells (1). This appears reasonable from a metabolic standpoint; since fatty acids are abundant in LNs and more ATP can be produced using fatty acids as a substrate, upregulation of FAO would be beneficial for survival, growth and invasion of metastatic cancer cells. Then how do cells decide whether to activate glycolysis or FAO? Since, in addition to TEAD, YAP interacts with multiple transcription factors, including FOXO1, HIF1α/β, KLF5, C/EBPα, and PPARγ (10), it is possible that YAP stimulates either glycolysis or FAO depending upon the availability of active transcription factors in the nucleus, which could be cell type-specific or affected by post-translational modification of transcription factors through upstream signaling mechanisms. Interestingly, gene set enrichment analyses suggest that the PPARα signaling pathway is activated in LN-metastatic cancer cells (1), and a previous study showed that bile acids upregulate PPARα in hepatoma HepG2 cells (16). Thus, it is tempting to speculate that YAP promotes FAO through interaction with PPARα. Since PPARα positively regulates bile acid synthesis (17), it is possible that bile acids, YAP, and PPARα may form an autocrine positive feedback mechanism to facilitate adaptation and spreading of metastatic cancer cells in the local environment of LNs. It is unclear whether elevated bile acids alone are sufficient to achieve activation of downstream transcription factor(s) to upregulate FAO or whether additional stimuli are necessary. Further investigation is needed to clarify the signaling mechanisms controlling tumor metastasis to LNs.

In summary, the study by Lee et al. shows that the bile acids-YAP pathway mediates metabolic flexibility, which confers adaptivity to the local environment and boosts the metastatic ability of cancer cells in local LNs (Figure 1) (1). The authors’ findings suggest that inhibition of YAP or FAO may represent a new therapeutic target to prevent survival and growth of metastatic cancer cells in LNs. Alternatively, an intervention to locally prevent activation of YAP in LNs may also be effective. Further investigation is warranted to clarify the mechanism by which YAP is regulated locally and how increased FAO affects downstream cellular function in metastatic cancer cells so that more therapeutic options for the attenuation of tumor metastasis may be identified.


Acknowledgments

Funding: This work was supported in part by U.S. Public Health Service Grants HL67724, HL91469, HL112330, HL138720, and AG23039 (J Sadoshima), and by the Foundation of Leducq Transatlantic Network of Excellence 15CBD04 (J Sadoshima). T Kashihara has been supported by a Postdoctoral Fellowship from the Uehara Memorial Foundation.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.


References

  1. Lee CK, Jeong SH, Jang C, et al. Tumor metastasis to lymph nodes requires YAP-dependent metabolic adaptation. Science 2019;363:644-9. [Crossref] [PubMed]
  2. Riggi N, Aguet M, Stamenkovic I. Cancer Metastasis: A Reappraisal of Its Underlying Mechanisms and Their Relevance to Treatment. Annu Rev Pathol 2018;13:117-40. [Crossref] [PubMed]
  3. Fidler IJ, Poste G. The "seed and soil" hypothesis revisited. Lancet Oncol 2008;9:808. [Crossref] [PubMed]
  4. Pavlova NN, Thompson CB. The Emerging Hallmarks of Cancer Metabolism. Cell Metab 2016;23:27-47. [Crossref] [PubMed]
  5. Warburg O. On respiratory impairment in cancer cells. Science 1956;124:269-70. [PubMed]
  6. Jia D, Lu M, Jung KH, et al. Elucidating cancer metabolic plasticity by coupling gene regulation with metabolic pathways. Proc Natl Acad Sci U S A 2019;116:3909-18. [Crossref] [PubMed]
  7. van Weverwijk A, Koundouros N, Iravani M, et al. Metabolic adaptability in metastatic breast cancer by AKR1B10-dependent balancing of glycolysis and fatty acid oxidation. Nat Commun 2019;10:2698. [Crossref] [PubMed]
  8. Wang YN, Zeng ZL, Lu J, et al. CPT1A-mediated fatty acid oxidation promotes colorectal cancer cell metastasis by inhibiting anoikis. Oncogene 2018;37:6025-40. [Crossref] [PubMed]
  9. Lovisa S, Kalluri R. Fatty Acid Oxidation Regulates the Activation of Endothelial-to-Mesenchymal Transition. Trends Mol Med 2018;24:432-4. [Crossref] [PubMed]
  10. Koo JH, Guan KL. Interplay between YAP/TAZ and Metabolism. Cell Metab 2018;28:196-206. [Crossref] [PubMed]
  11. Zhang X, Zhao H, Li Y, et al. The role of YAP/TAZ activity in cancer metabolic reprogramming. Mol Cancer 2018;17:134. [Crossref] [PubMed]
  12. Han S, Li T, Ellis E, et al. A novel bile acid-activated vitamin D receptor signaling in human hepatocytes. Mol Endocrinol 2010;24:1151-64. [Crossref] [PubMed]
  13. Liu R, Li X, Hylemon PB, et al. Conjugated Bile Acids Promote Invasive Growth of Esophageal Adenocarcinoma Cells and Cancer Stem Cell Expansion via Sphingosine 1-Phosphate Receptor 2-Mediated Yes-Associated Protein Activation. Am J Pathol 2018;188:2042-58. [Crossref] [PubMed]
  14. Anakk S, Bhosale M, Schmidt VA, et al. Bile acids activate YAP to promote liver carcinogenesis. Cell Rep 2013;5:1060-9. [Crossref] [PubMed]
  15. Lamar JM, Stern P, Liu H, et al. The Hippo pathway target, YAP, promotes metastasis through its TEAD-interaction domain. Proc Natl Acad Sci U S A 2012;109:E2441-50. [Crossref] [PubMed]
  16. Pineda Torra I, Claudel T, Duval C, et al. Bile acids induce the expression of the human peroxisome proliferator-activated receptor alpha gene via activation of the farnesoid X receptor. Mol Endocrinol 2003;17:259-72. [Crossref] [PubMed]
  17. Xie C, Takahashi S, Brocker CN, et al. Hepatocyte peroxisome proliferator-activated receptor alpha regulates bile acid synthesis and transport. Biochim Biophys Acta Mol Cell Biol Lipids 2019;1864:1396-411. [Crossref] [PubMed]
doi: 10.21037/biotarget.2019.08.01
Cite this article as: Kashihara T, Zablocki D, Sadoshima J. YAP-dependent metabolic remodeling in local lymph node boosts the function of cancer cells. Biotarget 2019;3:14.