Therapeutic targeting of oncogenic KRAS in pancreatic cancer by engineered exosomes
Editorial

Therapeutic targeting of oncogenic KRAS in pancreatic cancer by engineered exosomes

Theresa L. Whiteside

Departments of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, UPMC Hillman Cancer Center, Pittsburgh, PA, USA

Correspondence to: Theresa L. Whiteside, PhD, MDHC. Professor of Pathology, Immunology and Otolaryngology, University of Pittsburgh Cancer Institute, 5117 Centre Avenue, Suite 1.27, Pittsburgh, PA 15213, USA. Email: whitesidetl@upmc.edu.

Provenance: This is an invited Editorial commissioned by Section Editor Dr. Liping Li (Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institute of Health, Bethesda, MD, USA).

Comment on: Kamerkar S, LeBleu VS, Sugimoto H, et al. Exosomes facilitate therapeutic targeting of oncogenic KRAS in pancreatic cancer. Nature 2017;546:498-503.


Submitted Sep 27, 2017. Accepted for publication Oct 10, 2017.

doi: 10.21037/tcr.2017.10.32


Exosomes, the smallest (30–150 nm in diameter) subset of extracellular vesicles (EVs) are derived from the endocytic compartment of the parent cell and function as an inter-cellular communication system (1). The system operates in unicellular as well as multicellular organisms (2) and involves the transfer of signals and/or genetic messages from the parent to recipient cells (3). The mechanisms responsible for the message delivery to recipient cells have been intensively investigated and found to vary from the receptor/ligand-type uptake to macropinocytosis, endocytosis, or phagocytosis (4). The nature of recipient cells seems to determine the mechanism of exosome uptake. Tumor cells, including pancreatic adenocarcinomas, readily uptake exosomes engaging one or more of these mechanisms. Exosomes carry a rich cargo of integrins and opsonins that facilitate their uptake (5). In vivo, the time exosomes spend in the circulation is another factor that regulates their uptake. The removal of exosomes from the circulation by cells of the reticuloendothelial system (RES) is likely to be rapid, potentially interfering with the targeted delivery of the exosome cargo to recipient cells.

Exosomes are considered to be promising delivery vehicles for therapeutic agents such as, e.g., RNA interference (RNAi) (6). It appears that exosomes, like liposomes, can be readily loaded with RNAi. Because exosomes carry proteins enhancing their uptake, it was assumed that they would efficiently deliver RNAi to targeted recipient cells. However, enhanced exosome phagocytosis by monocytes/macrophages represents a potential hurdle of rapid exosome clearance from the circulation that might interfere with the intended RNAi delivery to target cells. In a recent paper published in Nature (7), Kamerkar and his group report that exosomes derived from fibroblast-like mesenchymal cells carry CD47, an immunoglobulin-like domain-containing molecule that serves as a “don’t eat me” signal. The binding of CD47 located on the exosome surface to its receptor, signal regulatory protein alpha (SIRPα), on phagocytic cells inhibits phagocytic functions (8). CD47 is broadly expressed on various types of tumor cells and normal tissue cells, and the antibody-mediated blockade of its tumor-protective functions has been used as therapy in patients with cancer (9). Similar to protecting tumor cells from phagocytosis, CD47 on exosomes contributes to suppression of their clearance and increases the efficiency of targeted content delivery. In a series of elegant experiments, the authors of the Nature paper successfully electroporated CD47high exosomes with Alexa Fluor 647 (AF647)-labeled short interfering RNA (siRNA), creating “iExosomes”. These exosomes delivered intraperitoneally (IP) to CD57BL/6 or nude mice showed better retention in the circulation and better accumulation in the liver, lung and pancreas than liposomes. Importantly, CD47 knockout (KO) exosomes showed significantly less retention, suggesting that CD47 presence on exosomes limits their clearance by circulating SIRPα+CD11+ monocytes. In the presence of blocking anti-CD47 antibody, disrupting the CD47-SIRPα signaling in monocytes, a significant increase of AF647+CD11b+ monocytes (i.e., monocytes internalizing labeled exosomes) in the circulation was observed. When CD47high iExosomes were injected into mice, a decrease in circulating AF647+CD11b+ monocytes was evident, suggesting that exosome escape from clearance by monocytes was partly mediated by the CD45/SIRPα signal.

The objective of the above-described iExosome delivery studies was to pave the way for implementation of RNAi-based therapy targeting oncogenic KRAS in pancreatic ductal adenocarcinoma (PDAC). Earlier studies suggested that oncogenic RAS upregulated macropinocytosis in pancreatic cancer cells facilitating exosome uptake. The investigators electroporated exosomes with siRNA or short hairpin RNA (shRNA) targeting KRASG12D and showed that these iExosomes were internalized by human PANC-1 cells and significantly decreased KRASG12D mRNA levels and RAS activity in these cells. This effect was specific, as cells containing wild-type KRAS were not altered. In the next series of experiments, mice with luciferase expressing orthotopic PANC-1 tumors were treated with repeated IP injections of iExosomes or iLiposomes (108 every other day). Tumors treated with iExosomes were significantly reduced in size relative to controls, and overall survival of mice was significantly improved. iLiposomes were less effective. The anti-tumor efficiency of iExosomes was significantly inhibited by blocking the CD47-SIRPα “don’t eat me” signal. Further, CD47 KO iExosomes did not robustly suppress tumor growth or prolong survival. The in vivo experiments in several different mouse models of pancreatic cancer confirmed the remarkable therapeutic efficacy of iExosomes that far surpassed that of liposomes. In additional in vivo experiments, the authors of the Nature paper also showed that iExosomes generated from mouse or human sources delivered to animals bearing advanced pancreatic tumors reduced tumor burden, decreased pancreatic desmoplasia, suppressed proliferation and enhanced apoptosis of cancer cells, reduced ERK phosphorylation, AKT phosphorylation and RAS levels as well as oncogenic KRASG12D expression with increased animal survival.

The reported significant advantages of therapy with engineered iExosomes targeting oncogenic KRAS in advanced PDAC in mice are especially impressive in light of the evidence that the RAS pathway is poorly druggable (10). What accounts for this impressive therapeutic potential of iExosomes that extended to advanced metastatic disease in this study? And why is iExosome therapeutically superior to iLiposome? The authors suggest that a longer retention of iExosomes in the circulation due to the CD47 content, the RAS-mediated enhanced micropinocytosis in tumor cells, and the presence in the iExosome cargo of proteins facilitating uptake by recipient tumor cells might have accounted for the observed improved therapeutic efficacy of iExosomes vs. iLiposomes. To test the first possibility, the authors could have further evaluated the role of CD47 in this process by decorating liposomes with CD47 and following their delivery and therapeutic effects. However, the clue to superior therapeutic effects of iExosomes may be more complex. While CD47 is the best known “don’t eat me” protein, there are bound to be others on the surface of various cells and carried by exosomes. The likely presence in the circulation of monocyte-derived SIRPα+ exosomes could antagonize the “don’t eat me” exosome-to-monocyte signaling (11). Further, there are numerous known “pro-eat me” molecules, including calreticulin or phosphatidyl serine or other pro-apoptotic proteins on tumor cells (12) and on exosomes these cells produce. Hence, the balance of exosomal “pro-eat me” vs. “don’t eat me” exosome components will surely impact on iExosomes retention in the circulation vs. their uptake by recipient cell. The exosome content of adhesion molecules is rich and varied as is the membrane content of specific ligands and receptors they carry, potentially resulting in differences in the exosome uptake by recipient cells (13). The simultaneous delivery by exosomes of many cognate receptor/ligands to recipient cell surface and the resulting signaling represents a powerful and rapid message delivery system that may outperform the other uptake mechanisms. Hence, iExosomes naturally endowed with the roster of specific signaling proteins are likely to deliver more effective messages than synthetic liposomes. Finally, an exosome carries numerous biologically active molecules in its cargo that upon uptake by a recipient cell are necessary to facilitate message translation, which liposomes may or may not be able to do. Also, it is important to remember that cells of the RES may be able to discriminate between biologically-active exosomes and decorated liposomes, differentially regulating their retention in the circulation. This regulation could be altered in advanced neoplasia, where the RES is stressed and the clearance mechanisms are partially overextended.

The Nature study convincingly shows that therapy of PDAC with engineered iExosomes targeting oncogenic KRAS was effective in reducing tumor growth and was superior to therapy with similarly administered liposomes. It emphasizes the promising potential of iExosomes in cancer therapy. It comes short, however, of adequately explaining the reasons for the observed therapeutic efficacy of iExosomes. This, of course, is the key question that needs to be addressed prior to further translation of iExosome-based cancer therapy to the clinical setting.


Acknowledgements

Funding: This study was supported in part by NIH grants (No. RO-1 CA168628 and R21 CA205644) to TL Whiteside.


Footnote

Conflicts of Interest: The author has no conflicts of interest to declare.


References

  1. Lo Cicero A, Stahl PD, Raposo G. Extracellular vesicles shuffling intercellular messages: for good or for bad. Curr Opin Cell Biol 2015;35:69-77. [Crossref] [PubMed]
  2. Berleman J, Auer M. The role of bacterial outer membrane vesicles for intra- and interspecies delivery. Environ Microbiol 2013;15:347-54. [Crossref] [PubMed]
  3. Abels ER, Breakefield XO. Introduction to Extracellular Vesicles: Biogenesis, RNA Cargo Selection, Content, Release, and Uptake. Cell Mol Neurobiol 2016;36:301-12. [Crossref] [PubMed]
  4. Mulcahy LA, Pink RC, Carter DR. Routes and mechanisms of extracellular vesicle uptake. J Extracell Vesicles 2014.3. [PubMed]
  5. Atay S, Godwin AK. Tumor-derived exosomes: A message delivery system for tumor progression. Commun Integr Biol 2014;7:e28231. [Crossref] [PubMed]
  6. Vader P, Mol EA, Pasterkamp G, et al. Extracellular vesicles for drug delivery. Adv Drug Deliv Rev 2016;106:148-56. [Crossref] [PubMed]
  7. Kamerkar S, LeBleu VS, Sugimoto H, et al. Exosomes facilitate therapeutic targeting of oncogenic KRAS in pancreatic cancer. Nature 2017;546:498-503. [PubMed]
  8. Willingham SB, Volkmer JP, Gentles AJ, et al. The CD47-signal regulatory protein alpha (SIRPa) interaction is a therapeutic target for human solid tumors. Proc Natl Acad Sci U S A 2012;109:6662-7. [Crossref] [PubMed]
  9. Weiskopf K. Cancer immunotherapy targeting the CD47/SIRPalpha axis. Eur J Cancer 2017;76:100-9. [Crossref] [PubMed]
  10. Gysin S, Salt M, Young A, et al. Therapeutic strategies for targeting ras proteins. Genes Cancer 2011;2:359-72. [Crossref] [PubMed]
  11. Koh E, Lee EJ, Nam GH, et al. Exosome-SIRPalpha, a CD47 blockade increases cancer cell phagocytosis. Biomaterials 2017;121:121-9. [Crossref] [PubMed]
  12. Penberthy KK, Ravichandran KS. Apoptotic cell recognition receptors and scavenger receptors. Immunol Rev 2016;269:44-59. [Crossref] [PubMed]
  13. Singh A, Fedele C, Lu H, et al. Exosome-mediated Transfer of alphavbeta3 Integrin from Tumorigenic to Nontumorigenic Cells Promotes a Migratory Phenotype. Mol Cancer Res 2016;14:1136-46. [Crossref] [PubMed]
Cite this article as: Whiteside TL. Therapeutic targeting of oncogenic KRAS in pancreatic cancer by engineered exosomes. Transl Cancer Res 2017;6(Suppl 9):S1406-S1408. doi: 10.21037/tcr.2017.10.32