NCI Network on Biobehavioral Pathways in Cancer

These projects have been funded in whole or in part with federal funds from the National Cancer Institute, National Institutes of Health, under Contract No. HHSN261200800001E. This research was supported by the National Cancer Institute Network on Biobehavioral Pathways in Cancer.

National Cancer Institute - Network on Biobehavioral Pathways in Cancer

Overview

The National Cancer Institute Network on Biobehavioral Pathways in Cancer (NBBPC) accelerates the translation and communication of biobehavioral discoveries to advance clinical cancer care.

NBBPC is a consortium designed to support knowledge of the molecular and signaling pathways that link psychological, behavioral, and social factors to cancer biology and apply that knowledge toward the development of efficacious interventions to reduce cancer risk and improve clinical outcomes. NBBPC has specific interest in proof-of-concept basic and translational studies to control disease in cancer patients, prevent recurrence post-treatment, and augment disease-free survival.

September 16, 2016 – Capstone Meeting Held for the Network on Biobehavioral Pathways in Cancer

Five years ago, a handful of cancer researchers with training in cell biology, psychology, public health, and related fields, set out to study the pathways that link psychological, behavioral, and social factors to cancer. Of particular interest, was whether stress and other psychological phenomena caused tumors to grow larger – and whether behaviors such as exercise or social engagement improved outcomes. The National Cancer Institute (NCI) Basic Biobehavioral and Psychological Sciences Branch led the effort to explore how psychological phenomena might be affecting the biology of cancer and disease outcomes via the Network on Biobehavioral Pathways in Cancer. On September 16, Network-funded researchers gathered at NCI-Shady Grove to deliver their findings.

Mission

The Network fosters research excellence through the integration and dissemination of relevant scientific discoveries and the identification, support, and communication of new research directions in the field of biobehavioral pathways in cancer.

Priorities

  • Stimulate novel scientific concepts and paradigms
  • Foster innovative collaborations between diverse disciplines
  • Disseminate relevant discoveries through major scientific conferences and meetings
  • Accelerate the translation of discoveries to patient benefit
  • Synthesize the state of the science, analyze secondary data, and publish
  • Encourage established scientists to apply their expertise to this emerging area of research
  • Cultivate the education, training, and professional advancement of early career scientists

NBBPC Members

NBBPC members provide the following:

  1. Foster the discovery-to-translation continuum of research related to biobehavioral pathways in cancer;
  2. Focus on unmet, understudied, highly exploratory questions that can’t yet be addressed through the submission of a research project grant application to NCI; and
  3. Develop and conduct proof of concept/principal/feasibility studies in support of the near term submission of research project grant applications to NCI.

The Network leverages and integrates expertise in cancer, stress, and cell biology; neuroscience; health behavior; psychology; social science; and oncology to advance the understanding of biological pathways that link behavioral processes and cancer.

The Network supports research in brain pathways that underlie psychological and social experiences, and their neurobiological impact on cancer via the sympathetic nervous system.

Scientific Steering Committee

Linda Alexander, Ph.D. Linda Alexander, Ph.D. exit disclaimer
Associate Dean for Academic Affairs
Professor, Social and Behavioral Sciences
West Virginia University
Steve Cole, Ph.D. Steve Cole, Ph.D. exit disclaimer
Associate Professor
David Geffen School of Medicine
University of California, Los Angeles
Susan K. Lutgendorf, Ph.D. Susan K. Lutgendorf, Ph.D. exit disclaimer
Professor & Starch Faculty Fellow
Department of Psychology
University of Iowa
Paige Green, Ph.D., M.P.H. Paige Green, Ph.D., M.P.H. exit disclaimer
Chief
Basic Biobehavioral and Psychological Sciences Branch
National Cancer Institute
Anil K. Sood, M.D.Anil K. Sood, MD exit disclaimer
Director, Professor
Dept. of Gynecologic Oncology and Cancer Biology
M.D. Anderson Cancer Center

Current Members

Michael H. Antoni, Ph.D.
Shamgar Ben-Eliyahu, Ph.D.
Nathan A. Berger, MD
Julienne Bower, Ph.D.
Erin Costanzo, Ph.D.
Naomi Eisenberger, Ph.D.
Wenwei Hu, Ph.D.
Jennifer M. Knight, MD
Don Lamkin, Ph.D.
Kelley S. Madden, Ph.D.
Tor Wager, Ph.D.

For inquiries about the Network mission and scientific scope, contact: Paige Green at 240-276-6899 and greenpa@nih.gov


Heuristic framework for research on biobehavioral risk factor influences on clinical cancer course.

Green, P., O’Connell, M., & Lutgendorf, S.K. (2013). Psychoneuroimmunology and cancer: A decade of discovery, paradigm shifts, and methodological innovations. Brain, Behavior, and Immunity, 30, S1-S9.

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Heuristic framework for research on biobehavioral risk factor influences on clinical cancer course.

Pilot Project Descriptions

Chart of projects for Biohehavioral Pathways in Cancer

Effects of Cognitive Behavioral Stress Management Intervention on Clinical Disease Endpoints in Women with Breast Cancer

Michael H. Antoni, Ph.D., University of Miami exit disclaimer

This project consists of extensive follow-up of a randomized, controlled trial, which aims to test the effects of group-based cognitive behavioral stress management intervention versus psychoeducational control on clinical disease endpoints over an extended time in women initially treated for non-metastatic breast cancer. It examines whether specific biobehavioral and psychological adaptation processes modified by the intervention in the first year of medical treatment predict differences in clinical endpoints (e.g., survival and recurrence) up to 13 years later.

Cognitive Behavioral Stress Management Intervention (University of Miami)

Stagl, J.M., Lechner, S.C., Carver, C.S., Bouchard, L.C., Gudenkauf, L.M., Jutagir, D.R., Diaz, A., Yu, Q., Blomberg, B.B., Ironson, G., Glück, S., Antoni, M.H. A randomized controlled trial of cognitive-behavioral stress management in breast cancer: survival and recurrence at 11-year follow-up. Breast Cancer Res Treat. 2015. Nov; 154(2):319-28.

Perioperative Use of Beta-blocker and COX2 Inhibitor

Shamgar Ben-Eliyahu, Ph.D., Tel Aviv University exit disclaimer

This project uses multicenter randomization to assess the short-term effects of counteracting excess perioperative catecholamine and prostaglandin levels on immune, endocrine, and pro-metastatic serum and histological indices. Results of this project will be used to develop a large-scale clinical trial.

Behavioral Pathways in Stem Cell Transplantation: CD14+ Gene Expression

Erin Costanzo, Ph.D., University of Wisconsin, Madison exit disclaimer

This project examines gene expression patterns of CD14+ cells as a potential pathway by which stress-related psychosocial factors may influence immune recovery and clinical outcomes following hematopoietic stem cell transplantation (HSCT). The study focuses on multiple myeloma patients recovering from autologous HSCT, given evidence for the role of CD14+ derived macrophages in immune recovery as well as in angiogenesis, apoptosis, and production of disease-promoting cytokines in this population.

Behavioral Pathways in Stem Cell Transplantation (University of Wisconsin, Madison)

Costanzo, E. S., Hematti, P., Callander, N. S., Coe, C. L., Juckett, M. B., Arevalo, J., Ma, J., Kim, J., Nelson, A. M., & Cole, S. W. (2015, March). Social attachment predicts monocyte gene expression profiles among individuals with multiple myeloma undergoing autologous stem cell transplantation. Paper presented at the 73rd Annual Meeting of the American Psychosomatic Society, Savannah, GA.

Neural Substrates of Social Support

Naomi Eisenberger, Ph.D., University of California, Los Angeles exit disclaimer

This project produced a white paper that served as the basis for the fMRI probe optimization study. The paper provides a literature review of fMRI-based research on behavioral probe paradigms and empirical neural activity correlates of social support, attachment, affiliation, and related psychological constructs. See Eisenberger, N. (2013). An Empirical Review of the Neural Underpinnings of Receiving and Giving Social Support: Implications for Health. Psychosomatic Medicine, 75(6):545–556. https://www.ncbi.nlm.nih.gov/pubmed/23804014

Neural Substrates of Social Support project (University of California, Los Angeles)

Eisenberger, N. (2013). An empirical review of the neural underpinnings of receiving and giving social support: Implications for health. Psychosomatic Medicine, 75(6):545–556.

fMRI Probe Optimization Study of Social Support

Naomi Eisenberger, Ph.D., and Julienne Bower, Ph.D., University of California, Los Angeles exit disclaimer

Based on the white paper referenced above, this project aims to identify and pilot test fMRI probe tasks that can help assess whether individual differences in measures of experienced social support (as measured by the Social Provisions Scale-Attachment and the UCLA Loneliness Scale) relate systematically to individual differences in neural activity to the specialized probe tasks. Phase I of the project will be conducted in healthy volunteer subjects.

fMRI Probe Optimization Study of Social Support project (University of California, Los Angeles)

Inagaki, T.K., Byrne Haltom, K.E., Suzuki, S., Jevtic, I., Hornstein, E, Bower, J.E., & Eisenberger, N.I. (2016) The neurobiology of giving versus receiving support: The role of stress-related and social reward–related neural activity. Psychosomatic Medicine, 78(4) p 443–453.

Stress and Tumorigenesis in Normal and p53 Knockout Models

Wenwei Hu, Ph.D., Robert Wood Johnson Foundation exit disclaimer

This project is investigating the impact of chronic stress on DNA damage accumulation, which, in keeping with the established chronic stress mouse model system, then promotes tumor initiation. Based on the recent finding that chronic stress attenuates the function of p53, a central player in tumor suppression, this project will test whether chronic stress promotes DNA damage, enhances mutation frequency and copy number variation in a largely p53-dependent manner.

Beta-Adrenergic Regulation of Acute Lymphocytic Leukemia

Don Lamkin, Ph.D., University of California, Los Angeles

This project examines a potential downstream mechanism by which beta-adrenergic signaling accelerates progression of acute lymphoblastic leukemia (ALL). Specifically, an orthotopic mouse model of human leukemia will be used to understand the role of the CXCR4- CXCL12 chemokine system in stress-enhanced ALL progression.

Metabolic Fingerprint of Stress Influences in Cancer

Anil K. Sood, MD, MD Anderson Cancer Center exit disclaimer

This project examines unique metabolic signatures in epithelial ovarian cancer tissues from human subjects with different depression and social support profiles. Global biochemical profiles were studied in tissue samples (n=85) from patients who are categorized according to scores on biobehavioral risk factors. Mechanistic and biological studies to examine the regulation of metabolic pathways in the context of chronic stress effects on the tumor microenvironment were also conducted.

Metabolic Fingerprint of Stress Influences on Cancer (MD Anderson Cancer Center)

Zand, B., Previs, R.A., Zacharias, N.M., Rupaimoole, R., Nagaraja, A.S., Guindani, M., Dalton, H.J., Hu, W., Pecot, C.V., Ivan, C., Wu, S.Y., McCullough, C.R., Gharpure, K.M., Shoshan, E., Pradeep, S., Mangala, L.S., Rodriguez-Aguayo, C., Taylor, M., Wang, Y., Nick, A.M., Davies, M.A., Armaiz-Pena, G., Liu, J., Lutgendorf, S.K., Baggerly, K.A., Bar, Eli M., Lopez-Berestein, G., Bhattacharya, P.K., Sood, A.K. Role of increased n-acetylaspartate levels in ovarian carcinoma. JNCI (2016) 108 (6): djv426

Rupaimoole, R., Previs, R.A., Lee, J., Pradeep, S., Wu, S.Y., Ivan, C., Ferracin, M., Dennison, J.B., Zacharias Millward, N.M., Nagaraja, A.S., Gharpure, K.M., McGuire, M., Sam, N., Armaiz-Pena, G.N., Sadaoui, N.C., Rodriguez-Aguayo, C., Calin, G.A., Drapkin, R.I., Mills, G.B., Zhang, W., Lopez-Berestein, G., Bhattacharya, P.K., Sood, A.K. Long noncoding RNA ceruloplasmin promotes cancer growth by altering glycolysis. Cell Reports ( 2015); 13(11):2395-402.

Nagaraja, A.S., Dorniak, P.L., Sadaoui, N.C., Kang, Y., Armaiz-Pena, G., Wu, S.Y., Rupaimoole, R., Allen, J.K., Pradeep, S., Zand, B., Previs, R., Hansen, J.M., Yang, P., Rodriguez-Aguayo, C., Lopez-Berestein, G., Lutgendorf, S.K., Cole, S.W., Sood, A.K. Sustained adrenergic signaling leads to increased metastasis in ovarian cancer via increased PGE2 synthesis. Oncogene (2015) 00, 1–8.

Watkins, J.L., Thaker, P.M., Nick, A.M., Ramondetta, L.M., Kumar, S., Urbauer, D.L., Matsuo, K., Squires, K.C., Coleman, R.L., Lutgendorf, S.K., Ramirez, P.T., and Sood, A.K. Clinical impact of selective and nonselective beta-blockers on survival in patients with ovarian cancer. Cancer 2015; 121:3444-51.

Interactive Wiki Page

Tor Wager, Ph.D., University of Colorado, Boulder exit disclaimer

This project provides a targeted literature review of fMRI-based research on brain stem control of sympathetic nervous system (SNS) activity, and its regulation by higher brain (e.g., cortical) regions. The interactive wiki page (https://canlabweb.colorado.edu/brainstemwiki/ exit disclaimer) identifies cortical and sub-cortical brain regions of interest and the relevant fMRI probe paradigm tasks suitable for use in subsequent studies relating social support to SNS activation.

Interactive Wiki Page (University of Colorado, Boulder)

Brainstem anatomy WIKI (https://canlabweb.colorado.edu/brainstemwiki/ exit disclaimer)

Biobehavioral Benefits of Mixed Gender Housing on Survival of Mice with Colon Neoplasia

Nathan A. Berger, MD, Case Western Reserve University exit disclaimer

To determine mechanisms and provide potential targets for design and implementation of biobehavioral interventions in cancer patients and survivors, this project examines the effect of (1) mixed gender housing, (2) same gender housing, and (3) social isolation on survival and changes in circulating hormones, cytokines, and other mediators and biomarkers in C57BL6J mice bearing the APCMin mutation predisposing to gastrointestinal neoplasia.

Dual Psychosocial Stressor Exposure and Spontaneous Breast Tumor Metastasis in MMTV-PyMT Mice: Does Dual Stressor Exposure Increase Metastasis by Regulating Circulating Exosomes and Tumor Extracellular Matrix?

Kelley S. Madden, Ph.D., University of Rochester exit disclaimer

This project will establish how exposure to a dual stressor is linked to metastasis in MMTV-PyMT mice, a spontaneous breast cancer model that mimics metastatic breast cancer in humans. The stressor, a combination of chronic psychological stress (social isolation) and acute restraint stress, may mimic the complex stressors experienced by cancer patients. This project examines distinct and novel biological mechanisms underlying stress exposure: (1) circulating exosomes, a newly defined metastatic mechanism, and (2) alterations in the tumor extracellular matrix.

Dual Psychosocial Stressor Exposure and Spontaneous Breast Tumor Metastasis in MMTV-pyMT Mice (University of Rochester)

Dawes, Ryan P., Daniel K. Byun, Edward B. Brown, Kelley S. Madden. “Psychosocial stress suppresses tumor progression in a murine model of spontaneous, metastatic breast cancer”. Psychoneuroimmunology Research Society (PNIRS) Annual Scientific Meeting. 2015. Seattle, Washington.

Invited Presentation

Roswell Park Cancer Institute (RPCI), Buffalo, NY. April 28, 2015. “Psychosocial Stress Exposure and Sympathetic Nervous System Activation in Preclinical Models of Breast Cancer”. Invited by Dr. Elizabeth Repasky, Professor of Immunology, RPCI.

Using Propranolol to Decrease Gene Expression of Stress- Mediated Beta-Adrenergic Pathways in Hematopoietic Stem Cell Transplant Recipients

Jennifer M. Knight, MD, Medical College of Wisconsin exit disclaimer

This project assesses whether gene expression of beta-adrenergic signaling pathways can be altered in individuals undergoing HSCT for multiple myeloma by administering a daily beta-blocker (propranolol). This is the first human trial of a beta-blocker to improve cancer control by pharmacologically intervening in biobehaviorally mediated gene expression. The goal is to leverage these findings for a larger, randomized controlled trial that evaluates clinical outcomes.