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Tunneling nanotubes: role in cancer progression? 
Emil Lou, M.D., Ph.D 
University of Minnesota 
ASCB/IFCB Annual Meeting 
Special Interest Session V – Tunneling Nanotubes, Cytonemes, and More 
December 6, 2014
•This research was presented as part of the Special Interest Subgroup V presentation entitled “Tunneling Nanotubes, Cytonemes, and More: Highways for Cell-to-Cell Communication from Development to Disease,” Saturday, December 6, 2014, at the 2014 ASCB/IFCB Annual Meeting in Philadelphia, Pennsylvania.
Following the conversation on #SocialMedia 
•Twitter: @cancerassassin1 
–I auto-tweeted this presentation, and use Twitter to share information on cancer research and clinical practice of oncology. 
–I used the conference hashtag #ASCB2014 for this session, which was Special Interest Subgroup V on Tunneling Nanotubes, Cytonemes, and More, at the ASCB 2014 Annual Meeting (12/6/2014). 
–The session was nicely summarized in a write-up by the team at Journal of Cell Biology: 
•http://jcb-biowrites.rupress.org/2014/12/ascb-2014-making-the-connection- between-cytonemes-and-tunneling-nanotubes.html 
•Links to all papers, Audioslide presentations, etc. are available on the Lou Lab website (umn.edu, search “Lou Lab”)
“Social Networking” in Cancer 
•Words to describe or characterize communicative activity between cancer cells: 
–Coordination – cell signaling; angiogenesis 
–Social activity – intercellular/intracellular communication; tumor-stromal interactions 
–Social networking – Gap junctions, Exosomes/Microvesicles, Tunneling Nanotubes 
–Synchronization – Cell cycle progression; cellular invasion 
–Coordinated expression – Altruistic Cell Death leading to resistance
Studying tumor cell advancement at the invasive front – modeling tumor invasion and recurrence through examination of TNTs 
Scratch assay of MSTO-211H (biphasic mesothelioma cells) – 22-hr time- lapse 
Lou et al., PLoS One, 2012 (online suppl video)
Cellular Dynamics, Networking, and Tumor Heterogeneity 
MSTO-211H cells connected in a syncytial network by TNTs Lou et al., PLoS One, 2012
Tumor microenvironment and the role of intercellular communication 
•Tumor heterogeneity 
–Molecular heterogeneity (e.g. microRNAs) 
–Cellular heterogeneity 
–Intratumoral vs inter-tumoral heterogeneity 
•Tumor-stroma proportions vary between tumor types, and even in the same type of cancer 
–Higher proportions have been associated with worse prognosis in several forms of solid tumor malignancies. 
•Long-distance communication 
–e.g. disruption of gap junctions upon EMT. 
–Malignant cells separated by dense tumor matrix in cases of tumors with high stromal density.
Lou et al., Pancreas, November 2013
Lou et al., PLoS One, 2012
Lou et al., PLoS One, 2012 - Figure 1
TnT formation is stimulated under conditions of physiologic stress
Figure 4, Lou et al., PLoS One, 2012
Brightfield time-lapse microscopy of formation of tunneling nanotubes in mesothelioma cell culture 
Lou et al., PLoS One, 2012 (video can be found in Supplementary Information online) 
MSTO-211H (biphasic mesothelioma cells) – brightfield time-lapse imaging every 15 minutes over 24 hours; video segment over 5-6 hours
From 2-D to 3-D study of nanotubes in human tumors 
Ady et al., Frontiers in Physiology, Oct 2014
Nanotubes in tumors from human mesothelioma and lung adenocarcinoma 
Lou et al., PLoS ONE, 2012
Thayanithy et al, Experimental Cell Research, 2014
Figure 5, Thayanithy et al., 
Exp Cell Res 2014 
1 
2 
3 
4
Thayanithy et al., 
Exp Cell Res 2014
Nanotubes in other tumors: 
Thayanithy, Dickson, Steer, Subramanian, and Lou. Published in Translational Research, 2014 
A), B) orthotopic syngeneic mouse model of osteosarcoma 
C) Human epithelial ovarian carcinoma
A “Nanotube Index”: Mesothelioma cells form TNTs at a higher rate compared with normal mesothelium 
Ady et al., Frontiers in Physiology, Oct 2014
TNT length may decrease over time 
Ady et al., Frontiers in Physiology, Oct 2014
Intercellular transfer of oncomiR-19a between osteosarcoma cells (A), and from osteosarcoma to osteoblasts (B) 
Thayanithy et al., Translational Research, 2014
SKOV 3 transfected with Alexa488-tagged miRNA 199a (green) transport to IOSE (normal) treated with DiD (red) via a TnT 
Thayanithy et al., Translational Research, 2014
Lou et al., Pancreas, November 2013
Ady et al., Frontiers in Physiology, 2014
Ady et al., Frontiers in Physiology, 2014
Ady et al., Frontiers in Physiology, 2014 (online video)
Research Team: 
The Lou Lab – Department of Medicine/Masonic Cancer Center, 
University of Minnesota: 
Venugopal Thayanithy, PhD – Research Associate/Postdoctoral Fellow 
Phillip Wong, MS – Research Technician 
Snider Desir – IBP Graduate Student 
Collaborators: 
University of Minnesota: 
Clifford Steer, MD – Department of Medicine 
Subbaya Subramanian, PhD – Department of Surgery 
MSKCC: Malcolm Moore, D.Phil; Katia Manova-Todorova, PhD; Sho Fujisawa, PhD 
City of Hope Cancer Center: Yuman Fong, MD 
Obstetrics & Gynecology, Division of Gynecologic Oncology: 
Elizabeth Dickson, MD – Gynecologic Oncology Fellow/Lou Lab Fellow 
Deanna Teoh, MD – Gynecologic Oncologist 
Melissa Geller, MD – Gynecologic Oncologist 
Peter Argenta, MD – Collaborator 
Biostatistics: Rachel Vogel Isaksson, M.S. and Chap Le, PhD
Funding Acknowledgements 
•UMN-CTSI KL2 Scholar Award 
•National Pancreas Foundation 
•American Cancer Society – IRG 
•Women’s Health Interdisciplinary Seed Grant, UMN Powell Center 
•AACR-GlaxoSmithKline Clinical Scholars Award 
•Minnesota Medical Foundation 
•Karen Wyckoff Rein in Sarcoma Foundation 
•Department of Medicine, Division of HOT 
•Baker Street Foundation

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ASCB annual meeting 2014 -Emil Lou - presentation at Subgroup V session on "Tunneling Nanotubes, Cytonemes, and More" 12-6-2014

  • 1. Tunneling nanotubes: role in cancer progression? Emil Lou, M.D., Ph.D University of Minnesota ASCB/IFCB Annual Meeting Special Interest Session V – Tunneling Nanotubes, Cytonemes, and More December 6, 2014
  • 2. •This research was presented as part of the Special Interest Subgroup V presentation entitled “Tunneling Nanotubes, Cytonemes, and More: Highways for Cell-to-Cell Communication from Development to Disease,” Saturday, December 6, 2014, at the 2014 ASCB/IFCB Annual Meeting in Philadelphia, Pennsylvania.
  • 3. Following the conversation on #SocialMedia •Twitter: @cancerassassin1 –I auto-tweeted this presentation, and use Twitter to share information on cancer research and clinical practice of oncology. –I used the conference hashtag #ASCB2014 for this session, which was Special Interest Subgroup V on Tunneling Nanotubes, Cytonemes, and More, at the ASCB 2014 Annual Meeting (12/6/2014). –The session was nicely summarized in a write-up by the team at Journal of Cell Biology: •http://jcb-biowrites.rupress.org/2014/12/ascb-2014-making-the-connection- between-cytonemes-and-tunneling-nanotubes.html •Links to all papers, Audioslide presentations, etc. are available on the Lou Lab website (umn.edu, search “Lou Lab”)
  • 4. “Social Networking” in Cancer •Words to describe or characterize communicative activity between cancer cells: –Coordination – cell signaling; angiogenesis –Social activity – intercellular/intracellular communication; tumor-stromal interactions –Social networking – Gap junctions, Exosomes/Microvesicles, Tunneling Nanotubes –Synchronization – Cell cycle progression; cellular invasion –Coordinated expression – Altruistic Cell Death leading to resistance
  • 5. Studying tumor cell advancement at the invasive front – modeling tumor invasion and recurrence through examination of TNTs Scratch assay of MSTO-211H (biphasic mesothelioma cells) – 22-hr time- lapse Lou et al., PLoS One, 2012 (online suppl video)
  • 6. Cellular Dynamics, Networking, and Tumor Heterogeneity MSTO-211H cells connected in a syncytial network by TNTs Lou et al., PLoS One, 2012
  • 7. Tumor microenvironment and the role of intercellular communication •Tumor heterogeneity –Molecular heterogeneity (e.g. microRNAs) –Cellular heterogeneity –Intratumoral vs inter-tumoral heterogeneity •Tumor-stroma proportions vary between tumor types, and even in the same type of cancer –Higher proportions have been associated with worse prognosis in several forms of solid tumor malignancies. •Long-distance communication –e.g. disruption of gap junctions upon EMT. –Malignant cells separated by dense tumor matrix in cases of tumors with high stromal density.
  • 8. Lou et al., Pancreas, November 2013
  • 9. Lou et al., PLoS One, 2012
  • 10. Lou et al., PLoS One, 2012 - Figure 1
  • 11. TnT formation is stimulated under conditions of physiologic stress
  • 12. Figure 4, Lou et al., PLoS One, 2012
  • 13. Brightfield time-lapse microscopy of formation of tunneling nanotubes in mesothelioma cell culture Lou et al., PLoS One, 2012 (video can be found in Supplementary Information online) MSTO-211H (biphasic mesothelioma cells) – brightfield time-lapse imaging every 15 minutes over 24 hours; video segment over 5-6 hours
  • 14. From 2-D to 3-D study of nanotubes in human tumors Ady et al., Frontiers in Physiology, Oct 2014
  • 15. Nanotubes in tumors from human mesothelioma and lung adenocarcinoma Lou et al., PLoS ONE, 2012
  • 16.
  • 17. Thayanithy et al, Experimental Cell Research, 2014
  • 18. Figure 5, Thayanithy et al., Exp Cell Res 2014 1 2 3 4
  • 19. Thayanithy et al., Exp Cell Res 2014
  • 20. Nanotubes in other tumors: Thayanithy, Dickson, Steer, Subramanian, and Lou. Published in Translational Research, 2014 A), B) orthotopic syngeneic mouse model of osteosarcoma C) Human epithelial ovarian carcinoma
  • 21. A “Nanotube Index”: Mesothelioma cells form TNTs at a higher rate compared with normal mesothelium Ady et al., Frontiers in Physiology, Oct 2014
  • 22. TNT length may decrease over time Ady et al., Frontiers in Physiology, Oct 2014
  • 23. Intercellular transfer of oncomiR-19a between osteosarcoma cells (A), and from osteosarcoma to osteoblasts (B) Thayanithy et al., Translational Research, 2014
  • 24. SKOV 3 transfected with Alexa488-tagged miRNA 199a (green) transport to IOSE (normal) treated with DiD (red) via a TnT Thayanithy et al., Translational Research, 2014
  • 25. Lou et al., Pancreas, November 2013
  • 26. Ady et al., Frontiers in Physiology, 2014
  • 27. Ady et al., Frontiers in Physiology, 2014
  • 28. Ady et al., Frontiers in Physiology, 2014 (online video)
  • 29. Research Team: The Lou Lab – Department of Medicine/Masonic Cancer Center, University of Minnesota: Venugopal Thayanithy, PhD – Research Associate/Postdoctoral Fellow Phillip Wong, MS – Research Technician Snider Desir – IBP Graduate Student Collaborators: University of Minnesota: Clifford Steer, MD – Department of Medicine Subbaya Subramanian, PhD – Department of Surgery MSKCC: Malcolm Moore, D.Phil; Katia Manova-Todorova, PhD; Sho Fujisawa, PhD City of Hope Cancer Center: Yuman Fong, MD Obstetrics & Gynecology, Division of Gynecologic Oncology: Elizabeth Dickson, MD – Gynecologic Oncology Fellow/Lou Lab Fellow Deanna Teoh, MD – Gynecologic Oncologist Melissa Geller, MD – Gynecologic Oncologist Peter Argenta, MD – Collaborator Biostatistics: Rachel Vogel Isaksson, M.S. and Chap Le, PhD
  • 30. Funding Acknowledgements •UMN-CTSI KL2 Scholar Award •National Pancreas Foundation •American Cancer Society – IRG •Women’s Health Interdisciplinary Seed Grant, UMN Powell Center •AACR-GlaxoSmithKline Clinical Scholars Award •Minnesota Medical Foundation •Karen Wyckoff Rein in Sarcoma Foundation •Department of Medicine, Division of HOT •Baker Street Foundation