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      Honami Naora Image

      Honami Naora, Ph.D.

      Department of Molecular Oncology, Division of Discovery Science

      In the News

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      What are neutrophils?

      Present Title & Affiliation

      Primary Appointment

      Professor (with tenure), Department of Molecular Oncology, Division of Discovery Science, University of Texas MD Anderson Cancer Center, Houston, TX

      Dual/Joint/Adjunct Appointment

      Faculty member, Graduate School of Biomedical Sciences, University of Texas MD Anderson Cancer Center/UT Health Houston

      Research Interests

      Research Interests

      1. Pre-Metastatic Niche Formation
      2. Metastatic Organotropism
      3. Immune and Non-Immune Cell Dynamics
      4. Tumor-Host Interactions
      5. Peritoneal Metastasis

      Research in the Naora Laboratory is directed to investigating the mechanisms of metastatic organotropism, with a focus on cellular dynamics in peritoneal metastasis. Whereas metastasis to various distal sites occurs through the blood circulation or lymphatic system, ovarian cancers and several other types of abdominal cancers often disseminate through the interstitial fluid in the peritoneal cavity.


      A common destination site of cancer cells that disseminate intraperitoneally is the omentum, an immune cell-rich fatty tissue that drapes from stomach. For decades, metastasis to the omentum has been regarded as a passive process that is governed by peritoneal fluid flow. However, we have discovered that metastatic tropism for the omentum is actively orchestrated by early-stage primary tumors. Our ongoing research seeks to address the following fundamental biological questions and unmet clinical needs.


      1. The omentum contains a high abundance of immune cell structures called fat-associated lymphoid clusters (FALCs) that play a critical role in eliminating pathogens from the peritoneal cavity. Paradoxically, cancer cells that shed into the peritoneal fluid are highly prone to form implants in omental FALCs. A major objective of our research is to understand why these FALCs do not effectively defend against cancer cells.


      2. Metastasis to the omentum leads to bowel obstruction. Omentectomy is the standard of care but it is difficult to resect the omentum in its entirety. By investigating the cellular dynamics in the omentum and peritoneal cavity, our ultimate goal is to develop strategies that can minimize the risk of colonization of preserved omental tissues by occult cancer cells.


      3. Omental metastasis is often detected after a bulky mass has formed. By delineating the mechanisms that orchestrate formation of the pre-metastatic niche in the omentum, our ultimate goal is to identify approaches that can detect tumors at an early, pre-metastatic stage.




      Education & Training

      Degree-Granting Education

      1994The Australian National University, Canberra, AU, Medical Sciences, Ph.D
      1990The Australian National University, Canberra, AU, Biochemistry, B.S. with First-Class Honors

      Postgraduate Training

      1999-2000Research Fellowship, Cancer immunology, Johns Hopkins University School of Medicine, Baltimore, MD
      1997-1998Research Fellowship, Immunology, Institut Pasteur, Paris
      1994-1997Research Fellowship, Cancer biology, The Australian National University, Canberra

      Experience & Service

      Faculty Academic Appointments

      Associate Professor (with tenure), Department of Molecular and Cellular Oncology, Division of Discovery Science, University of Texas MD Anderson Cancer Center, Houston, TX, 2013 - 2022

      Associate Professor (with tenure), Department of Systems Biology, Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, 2007 - 2013

      Assistant Professor (tenure-track), Department of Systems Biology, Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, 2004 - 2007

      Assistant Professor (tenure-track), Department of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, 2002 - 2004

      Research Associate (Research faculty appointment), Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, 2000 - 2002

      Intramural Institutional Committee Activities

      Member, ADVANCE committee (for Dr. Min Sup Song, Dept. of Molecular & Cellular Oncology), University of Texas MD Anderson Cancer Center, 2025

      Member, Margaret Kripke Legend Award Review Committee, University of Texas MD Anderson Cancer Center, 2025

      Member, Promotion and Tenure Committee (Research), University of Texas MD Anderson Cancer Center, 2024 - Present

      Member, GSBS Program Directors Committee, Graduate School of Biomedical Sciences, 2024 - Present

      Member, GSBS Graduate Program in Cancer Biology Steering Committee, Graduate School of Biomedical Sciences, 2024 - Present

      Chair, Education Committee of the Faculty Senate, University of Texas MD Anderson Cancer Center, 2024 - 2025

      Member, ADVANCE committee (for Dr. Ju-Seog Lee, Dept. of Systems Biology), University of Texas MD Anderson Cancer Center, 2024

      Member, ADVANCE committee (for Dr. Chunru Lin, Dept. of Molecular & Cellular Oncology), University of Texas MD Anderson Cancer Center, 2024

      Member, ADVANCE committee (for Dr. Liuqing Yang, Dept. of Molecular & Cellular Oncology), University of Texas MD Anderson Cancer Center, 2024

      Member, Graduate Education Committee, University of Texas MD Anderson Cancer Center, 2023 - 2025

      Member, Molecular & Cellular Oncology Chair Search Advisory Committee, University of Texas MD Anderson Cancer Center, 2023 - 2024

      Senator (Molecular & Cellular Oncology), Faculty Senate, University of Texas MD Anderson Cancer Center, 2022 - 2025

      Member, GSBS Program Directors Committee, Graduate School of Biomedical Sciences, 2022 - 2024

      Member, GSBS Graduate Program in Cancer Biology Steering Committee, Graduate School of Biomedical Sciences, 2022 - 2024

      Member, Education & Training Internal Advisory Board, University of Texas MD Anderson Cancer Center, 2022 - 2023

      Member, Institutional Strategic Plan Breakthroughs Cohorts 2 Committee, University of Texas MD Anderson Cancer Center, 2022

      Member, Faculty Appraisal Working Group, University of Texas MD Anderson Cancer Center, 2022

      Member, Faculty Workload Survey Working Group, University of Texas MD Anderson Cancer Center, 2022

      Member, Research Enablement, Activities and Conduct Team (REACT), University of Texas MD Anderson Cancer Center, 2021 - Present

      Co-Chair, Education Committee of the Faculty Senate, University of Texas MD Anderson Cancer Center, 2021 - 2024

      Member, Research Affairs Committee of the Faculty Senate, University of Texas MD Anderson Cancer Center, 2021 - 2022

      Member, Faculty Advisory Committee for Postdoctoral Fellows, University of Texas MD Anderson Cancer Center, 2021 - 2022

      Senator (Molecular & Cellular Oncology), Faculty Senate, University of Texas MD Anderson Cancer Center, 2020 - 2022

      Member, Executive Committee of the Faculty Senate, University of Texas MD Anderson Cancer Center, 2020 - 2022

      Member, Faculty Achievements Awards Committee, University of Texas MD Anderson Cancer Center, 2020

      Member, Faculty Achievement Awards Committee, University of Texas MD Anderson Cancer Center, 2019

      Member, GSBS Academic Standards Committee, Graduate School of Biomedical Sciences, 2018 - 2021

      Senator (Molecular & Cellular Oncology), Faculty Senate, University of Texas MD Anderson Cancer Center, 2017 - 2020

      Member, Institutional Research Grants Scientific Review Committee, University of Texas MD Anderson Cancer Center, 2017 - 2020

      Reviewer, INTEREST- Internal Review Study Section, University of Texas MD Anderson Cancer Center, 2017

      Member, Graduate Program in Cancer Biology, Faculty Membership Subcommittee, Graduate School of Biomedical Sciences, 2017

      Chair, Alfred G. Knudson Award Review Committee, Graduate School of Biomedical Sciences, 2015

      Senator (Molecular & Cellular Oncology), Faculty Senate, University of Texas MD Anderson Cancer Center, 2013 - 2016

      Member, Executive Committee of the Faculty Senate, University of Texas MD Anderson Cancer Center, 2013 - 2014

      Member, Institutional Biosafety Committee, University of Texas MD Anderson Cancer Center, 2013 - 2014

      Member, Division of Cancer Medicine Research Awards Committee, University of Texas MD Anderson Cancer Center, 2013

      Member, Division of Cancer Medicine Research Awards Committee, University of Texas MD Anderson Cancer Center, 2012

      Member, John P. McGovern Award Committee, Graduate School of Biomedical Sciences, 2012

      Member, T.C. Hsu Scholarship Committee, Graduate School of Biomedical Sciences, 2012

      Member, Division of Cancer Medicine Research Awards Committee, University of Texas MD Anderson Cancer Center, 2011

      Senator (Systems Biology), Faculty Senate, University of Texas MD Anderson Cancer Center, 2010 - 2013

      Chair, Graduate Program in Cancer Biology, International Students Admissions Subcommittee, Graduate School of Biomedical Sciences, 2009 - 2011

      Member, Institutional Research Grants Scientific Review Committee, University of Texas MD Anderson Cancer Center, 2007 - 2010

      Member, Institutional Biosafety Committee, University of Texas MD Anderson Cancer Center, 2006 - 2011

      Extramural Institutional Committee Activities

      Board member, Board of Directors, Asian American Academy of Science and Engineering, 2022 - Present

      Member, International Scientific Advisory Board, Ovarian Cancer Research Foundation, 2022 - Present

      Member, Advisory Board, HERA Ovarian Cancer Foundation, 2002 - 2009

      Editorial Activities

      Editorial Board Member, Journal of Cancer Biology and Treatment, 2014

      Editorial Board Member, Clinical Research and Development, 2014

      Honors & Awards

      2024Honoree, Education & Mentorship Advancement, University of Texas MD Anderson Cancer Center
      2003 - 2004Ovarian Cancer Research Fund Award, Ovarian Cancer Research Fund
      2003Eagle Award for Scientific Achievement, Cancer Fighters of Houston
      2000 - 2002Research Fellowship Award, Prevent Cancer Foundation (formerly Cancer Research Foundation of America)
      1997 - 1998Sidaction Fellowship, Fondation pour la Recherche Medicale, France
      1991Today's Life Science Award, Australian Society for Medical Research
      1990 - 1993Australian Postgraduate Research Award, Commonwealth Government of Australia
      1989Janet Elspeth Crawford Prize, The Australian National University

      Professional Memberships

      Asian American Academy of Science and Engineering

      2022 - Present

      American Association of University Professors

      2022 - Present

      International Society for Extracellular Vesicles

      2018 - Present

      Texas Faculty Association

      2010 - 2013

      American Association for Cancer Research

      1999 - Present

      Australia and New Zealand Society for Cell Biology

      1993 - 1997

      Australian Society of Immunology

      1993 - 1994

      Australian Society for Medical Research

      1991 - 1993

      Australian Society of Biochemistry and Molecular Biology

      1990 - 1997

      Selected Publications

      Peer-Reviewed Articles

      1. Lee W, Akasaka H, Naora H. Protocol for assessing mobilization of peritoneal B cells to the pre-metastatic omentum in an orthotopic mouse model of ovarian cancer. STAR Protoc, 2025. e-Pub 2025. PMID: 40327511.
      2. Lee W, Ko SY, Akasaka H, Weigert M, Lengyel E, Naora H. Neutrophil extracellular traps promote pre-metastatic niche formation in the omentum by expanding innate-like CD43+ B cells that express IL-10. Cancer Cell 43(1):69-85, 2025. e-Pub 2025. PMID: 39753138.
      3. Welsh JA, Goberdhan D, O'Driscoll L, Buzas E, Blenkiron C, Bussolati B, Cai H, Di Vizio D, Driedonks T, Erdbrügger U, Falcon-Perez J, Fu Q, Hill AF, Lenassi M, Kiang S, Lim SK, Mahoney MG, Mohanty S, Möller A, Nieuwland R, Ochiya T, Sahoo S, Torrecilhas A, Zheng L, Zijlstra A, Bergese P, Bridges EM, Brucale M, Burger D, Carney RP, Cocozza F, Cocucci E, Colombo F, Crescitelli R, Hanser E, Harris AH, Haughey NJ, Hendrix A, Ivanov AR, Kruh-Garcia NA, Kyburz D, Lässer C, Lötvall J, Martens E, Mizenko RR, Newman LA, Ridolfi A, Rohde E, Rojalin T, Rowland A, Sandau U, Saugstad J, Shekari F, Swift S, Ter-Ovanesyan D, Tosar J, Useckaite Z, Valle F, van Herwijnen M, Wauben M, Wehman A, Williams S, Zendrini A, Zimmerman A, MISEV Consortium, Théry C, Witwer KW. Minimal information for studies of extracellular vesicles (MISEV2023): from basic to advanced approaches. J Extracell Vesicles 13:e12451, 2024. e-Pub 2024. PMID: 38326288.
      4. Akasaka H, Lee W, Ko SY, Lengyel E, Naora H. Normal saline remodels the omentum and stimulates its receptivity for transcoelomic metastasis. JCI Insight 8:e167336, 2023. e-Pub 2023. PMID: 37345662.
      5. Ko SY, Lee W, Weigert M, Jonasch E, Lengyel E, Naora H. The glycoprotein CD147 defines miRNA-enriched extracellular vesicles that derive from cancer cells. J Extracell Vesicles 12(4):e12318, 2023. e-Pub 2023. PMID: 36973758.
      6. Lee W, Ko SY, Mohamed MSE, Kenny HA, Lengyel E, Naora H. Neutrophils facilitate ovarian cancer pre-metastatic niche formation in the omentum. J Exp Med 216(1):176-194, 2019. e-Pub 2019. PMID: 30567719.
      7. Ko SY, Lee W, Kenny HA, Dang LH, Ellis LM, Jonasch E, Lengyel E, Naora H. Cancer-derived small extracellular vesicles promote angiogenesis by heparin-bound, bevacizumab-insensitive VEGF, independent of vesicle uptake. Commun Biol 2:386, 2019. e-Pub 2019. PMID: 31646189.
      8. Trinh B, Ko SY, Haria D, Barengo N, Naora H. The homeoprotein DLX4 controls inducible nitric oxide synthase-mediated angiogenesis in ovarian cancer. Mol Cancer 14:e97, 2015. e-Pub 2015. PMID: 25924901.
      9. Trinh BQ, Barengo N, Kim SB, Lee JS, Zweidler-McKay PA, Naora H. The homeobox gene DLX4 regulates erythro-megakaryocytic differentiation by stimulating IL-1β and NF-κB signaling. J Cell Sci 128:3055-3067, 2015. e-Pub 2015. PMID: 26208636.
      10. Haria D, Trinh BQ, Ko SY, Barengo N, Liu J, Naora H. The homeoprotein DLX4 stimulates NF-κB activation and CD44-mediated tumor-mesothelial cell interactions in ovarian cancer. Am J Pathol 185:2298-2308, 2015. e-Pub 2015. PMID: 26067154.
      11. Ko SY, Ladanyi A, Lengyel E, Naora H. Expression of the homeobox gene HOXA9 in ovarian cancer induces peritoneal macrophages to acquire an M2 tumor-promoting phenotype. Am J Pathol 184:271-281, 2014. e-Pub 2014. PMID: 24332016.
      12. Ko SY, Naora H. HOXA9 promotes homotypic and heterotypic cell interactions that facilitate ovarian cancer dissemination via its induction of P-cadherin. Mol Cancer 13:170-178, 2014. e-Pub 2014. PMID: 25023983.
      13. Usui A, Ko SY, Barengo N, Naora H. P-cadherin promotes ovarian cancer dissemination through tumor cell aggregation and tumor-peritoneum interactions. Mol Cancer Res 12:504-513, 2014. e-Pub 2014. PMID: 24448686.
      14. Trinh BQ, Ko SY, Barengo N, Lin SY, Naora H. Dual functions of the homeoprotein DLX4 in modulating responsiveness of tumor cells to topoisomerase II-targeting drugs. Cancer Res 73:1000-1010, 2013. e-Pub 2013. PMID: 23222298.
      15. Ko SY, Barengo N, Ladanyi A, Lee JS, Marini F, Lengyel E, Naora H. HOXA9 promotes ovarian cancer growth by stimulating cancer-associated fibroblasts. J Clin Invest 122:3603-3617, 2012. e-Pub 2012. PMID: 22945634.
      16. Trinh BQ, Barengo N, Naora H. Homeodomain protein DLX4 counteracts key transcriptional control mechanisms of the TGF-β cytostatic program and blocks the antiproliferative effect of TGF-β. Oncogene 30:2718-2729, 2011. e-Pub 2011. PMID: 21297662.
      17. Zheng J, Chang B, Yang G, Rosen DG, Mills GB, Naora H, Auersperg N, Malpica A, Liu J. Induction of high grade serous carcinoma in human ovarian surface epithelial cells using combined genetic elements and peritoneal microenvironment. Cell Cycle 9:140-145, 2010. e-Pub 2010. PMID: 20016289.
      18. Ko SY, Lengyel E, Naora H. The Müllerian HOXA10 gene promotes growth of ovarian surface epithelial cells by stimulating epithelial-stromal interactions. Mol Cell Endocrinol 317:112-119, 2010. e-Pub 2010. PMID: 20036708.
      19. Ko SY, Guo H, Barengo N, Naora H. Inhibition of ovarian cancer growth by a tumor-targeting peptide that binds eukaryotic translation initiation factor 4E. Clin Cancer Res 15:4336-4347, 2009. e-Pub 2009. PMID: 19458052.
      20. Hara F, Samuel S, Liu J, Rosen D, Langley RR, Naora H. A homeobox gene related to Drosophila Distal-less promotes ovarian tumorigenicity by inducing expression of vascular endothelial growth factor and fibroblast growth factor-2. Am J Pathol 170:1595-1606, 2007. e-Pub 2007. PMID: 17456765.
      21. Yoshida H, Broaddus R, Cheng W, Xie S, Naora H. Deregulation of the HOXA10 homeobox gene in endometrial carcinoma: Role in epithelial-mesenchymal transition. Cancer Res 66:889-897, 2006. e-Pub 2006. PMID: 16424022.
      22. Cheng W, Liu J, Yoshida H, Rosen D, Naora H. Lineage infidelity of epithelial ovarian cancers is controlled by HOX genes that specify regional identity in the reproductive tract. Nat Med 11:531-537, 2005. e-Pub 2005. PMID: 15821746.
      23. Yoshida H, Liu J, Samuel S, Cheng W, Rosen D, Naora H. Steroid receptor coactivator-3, a homolog of Taiman that controls cell migration in the Drosophila ovary, regulates migration of human ovarian cancer cells. Mol Cell Endocrinol 245:77-85, 2005. e-Pub 2005. PMID: 16298470.
      24. Silver DL, Naora H, Liu J, Cheng W, Montell DJ. Activated signal transducer and activator of transcription (STAT) 3: localization in focal adhesions and function in ovarian cancer cell motility. Cancer Res 64:3550-3558, 2004. e-Pub 2004. PMID: 15150111.
      25. Yoshida H, Cheng W, Hung J, Montell D, Geisbrecht E, Rosen D, Liu J, Naora H. Lessons from border cell migration in the Drosophila ovary: A role for myosin VI in dissemination of human ovarian cancer. Proc Natl Acad Sci USA 101:8144-8149, 2004. e-Pub 2004. PMID: 15146066.
      26. Naora H, Yang Y, Montz FJ, Seidman JD, Kurman RJ, Roden RBS. A serologically identified tumor antigen encoded by a homeobox gene promotes growth of ovarian epithelial cells. Proc Natl Acad Sci USA 98:4060-4065, 2001. e-Pub 2001. PMID: 11274429.
      27. Naora H, Montz FJ, C-Y C, Roden RBS. Aberrant expression of homeobox gene HOXA7 is associated with müllerian-like differentiation of epithelial ovarian tumors and the generation of a specific autologous antibody response. Proc Natl Acad Sci USA 98:15209-15214, 2001. e-Pub 2001. PMID: 11742062.
      28. Russell L, Naora H, Naora H. Down-regulated RPS3a/nbl expression during retinoid-induced differentiation of HL-60 cells: a close association with diminished susceptibility to actinomycin D-stimulated apoptosis. Cell Struct Func 25:103-113, 2000. e-Pub 2000. PMID: 10885580.
      29. Naora H, Gougeon ML. Interleukin-15 is a potent survival factor in the prevention of spontaneous but not CD95-induced apoptosis in CD4 and CD8 T lymphocytes of HIV-infected individuals. Correlation with its ability to increase bcl-2 expression. Cell Death Differentiation 6:1002-1011, 1999. e-Pub 1999. PMID: 10556978.
      30. Naora H, Gougeon ML. Enhanced survival and potent expansion of the natural killer cell population of HIV-infected individuals by exogenous interleukin-15. Immunol Letts 68:359-367, 1999. e-Pub 1999. PMID: 10424444.
      31. Naora H, Gougeon ML. Activation, survival and apoptosis of CD45RO+ and CD45RO- T cells of HIV-infected individuals: Effects of interleukin-15 and comparison with interleukin-2. Immunology 97:181-187, 1999. e-Pub 1999. PMID: 10447730.
      32. Sorimachi K, Naora H, Akimoto K, Niwa A, Naora H. Multinucleation and preservation of nucleolar integrity of macrophages. Cell Biol Int 22:351-357, 1998. e-Pub 1998. PMID: 10198155.
      33. Naora H, Takai I, Adachi M, Naora H. Altered cellular responses by varying expression of a ribosomal protein gene: Sequential coordination of enhancement and suppression of ribosomal protein S3a gene expression induces apoptosis. J Cell Biol 141:741-753, 1998. e-Pub 1998. PMID: 9566973.
      34. Naora H, Seno S, Naora H. Regulation of tumor growth as a 'total mass' in mice: Apoptosis as a major mechanism in altering growth rates of single and multiple, co-existing tumor nodules. Pathol Int 48:730-738, 1998. e-Pub 1998. PMID: 9778112.
      35. Naora H, Nishida T, Shindo Y, Adachi M, Naora H. Antisense sequences of the nbl gene induce apoptosis in the human promyelocytic leukemia cell line HL-60. Leukemia 12:532-541, 1998. e-Pub 1998. PMID: 9557612.
      36. Naora H, Nishida T, Shindo Y, Adachi M, Naora H. Constitutively enhanced nbl expression is associated with the induction of internucleosomal DNA cleavage by actinomycin D. Biochem Biophys Res Comm 224:258-264, 1996. e-Pub 1996. PMID: 8694823.
      37. Naora H, Naora H. Differential expression patterns of β-actin mRNA in cells undergoing apoptosis. Biochem Biophys Res Comm 211:491-496, 1995. e-Pub 1995. PMID: 7794260.
      38. Naora H, Young IG. Comparison of the mechanisms regulating IL-5, IL-4 and three other lymphokine genes in the Th2 clone D10.G4.1. Exp Hematol 23:597-602, 1995. e-Pub 1995. PMID: 7601249.
      39. Naora H, Nishida T, Shindo Y, Adachi M, Naora H. Association of nbl gene expression and glucocorticoid-induced apoptosis in mouse thymus in vivo. Immunology 85:63-68, 1995. e-Pub 1995. PMID: 7635523.
      40. Minamide S, Naora H, Adachi M, Okano A, Naora H. Apoptosis as a mechanism of skin renewal: Ley-antigen expression is involved in an early event of a cell's commitment to apoptosis. Histochemistry 103:339-343, 1995. e-Pub 1995. PMID: 7543813.
      41. Naora H, Young IG. Mechanisms regulating the mRNA levels of interleukin-5 and two other coordinately expressed lymphokines in the murine T lymphoma EL4.23. Blood 83:3620-3628, 1994. e-Pub 1994. PMID: 8204886.
      42. Naora H, Altin JG, Young IG. TCR-dependent and -independent signaling mechanisms differentially regulate lymphokine gene expression in the murine T helper clone D10.G4.1. J Immunol 152:5691-5702, 1994. e-Pub 1994. PMID: 7911489.
      43. Naora H, Van Leeuwen BH, Bourke PF, Young IG. Functional role and signal-induced modulation of proteins recognizing the conserved TCATTT-containing promoter elements in the murine IL-5 and GM-CSF genes in T lymphocytes. J Immunol 153:3466-3475, 1994. e-Pub 1994. PMID: 7930569.

      Invited Articles

      1. Ko SY, Lee W, Naora H. Harnessing microRNA-enriched extracellular vesicles for liquid biopsy. Front Mol Biosci 11:1356780, 2024. e-Pub 2024. PMID: 38449696.
      2. Akasaka H, Naora H. Revisiting the use of normal saline for peritoneal washing in ovarian cancer. Int J Mol Sci 24:16449, 2023. e-Pub 2023. PMID: 38003636.
      3. Ko SY, Naora H. Extracellular vesicle membrane-associated proteins: emerging roles in tumor angiogenesis and anti-angiogenesis therapy resistance. Int J Mol Sci 21:5418, 2020. e-Pub 2020. PMID: 32751440.
      4. Lee W, Naora H. Neutrophils fertilize the pre-metastatic niche. Aging 11:6624-6625, 2019. e-Pub 2019. PMID: 31509520.
      5. Ko SY, Naora H. Adaptation of ovarian cancer cells to the peritoneal environment: Multiple mechanisms of the developmental patterning gene HOXA9. Cancer Cell Microenv 1:e379, 2014. e-Pub 2014. PMID: 26000332.
      6. Naora H. Heterotypic cellular interactions in the ovarian tumor microenvironment: Biological significance and therapeutic implications. Front Oncol 4:18-24, 2014. e-Pub 2014. PMID: 24567915.
      7. Ko SY, Naora H. Therapeutic strategies for targeting the ovarian tumor stroma. World J Clin Cases 2:194-200, 2014. e-Pub 2014. PMID: 24945005.
      8. Haria D, Naora H. Homeobox gene deregulation: Impact on the hallmarks of cancer. Cancer Hallm 1:67-76, 2013. e-Pub 2013. PMID: 24761365.
      9. Naora H. A peptide-based approach to inhibit the translational machinery in tumors. Chemistry Today 28:26-28, 2010. e-Pub 2010.
      10. Naora H. The heterogeneity of epithelial ovarian cancers: reconciling old and new paradigms. Expert Rev Mol Med 9:1-12, 2007. e-Pub 2007. PMID: 17477890.
      11. Naora H, Montell DJ. Ovarian cancer metastasis: Integrating insights from disparate model organisms. Nat Rev Cancer 5:355-366, 2005. e-Pub 2005. PMID: 15864277.
      12. Naora H. Developmental patterning in the wrong context: The paradox of epithelial ovarian cancers. Cell Cycle 4:86-88, 2005. e-Pub 2005. PMID: 16082202.
      13. Samuel S, Naora H. Homeobox gene expression in cancer: Insights from developmental regulation and deregulation. Eur J Cancer 41:2428-2437, 2005. e-Pub 2005. PMID: 16199152.
      14. Gougeon ML, Ledru E, Naora H, Bocchino M, Lecoeur H. HIV, cytokines and programmed cell death. A subtle interplay. Ann NY Acad Sci 926:30-45, 2000. e-Pub 2000. PMID: 11193039.
      15. Naora H, Naora H. Involvement of ribosomal proteins in regulating cell growth and apoptosis: Translational modulation or recruitment for extraribosomal activity?. Immunol Cell Biol 77:197-205, 1999. e-Pub 1999. PMID: 10361251.

      Editorials

      1. Akasaka H, Lee W, Naora H. The trap becomes the target: Molecular basis for targeted inhibition of neutrophil extracellular traps in the pre-metastatic niche. Expert Opin Ther Targets, 2025. PMID: 40632026.

      Book Chapters

      1. Naora H. Heterotypic cellular interactions in the ovarian tumor microenvironment. In: Advances in Epithelial Ovarian Cancer: Model Systems, Microenvironmental Influences, Therapy & Origins. Frontiers, 2016.
      2. Trinh BQ, Naora H. Homeobox genes and their functional significance in ovarian tumorigenesis. In: Ovarian Cancer: Basic Science Perspective. In-Tech Publishing, 2012.
      3. Hennessy BT, Carey M, Naora H, Mills GB. Ovarian Cancer: Molecular, Cellular and Clinical Biology. In: Ovarian Cancer: State of the Art. Remedica Medical Education & Publishing, 2008.

      Web Publications

      1. Naora H. Nature Behind the Paper Commentary. An uptake-independent mechanism of extracellular vesicles in tumor-stroma interactions and anti-angiogenic therapy resistance.
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