Skip to main content
  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

AACR logo

  • Register
  • Log in
  • My Cart
Advertisement

Main menu

  • Home
  • About
    • The Journal
    • AACR Journals
    • Journal Sections
    • Subscriptions
    • Permissions and Reprints
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • Collections
      • COVID-19 & Cancer Resource Center
      • Precision Medicine and Therapeutic Resistance
      • Clinical Trials
      • Immuno-oncology
      • Editors' Picks
      • "Best of" Collection
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • Editors' Picks
    • OnlineFirst
    • Citation
    • Author/Keyword
    • RSS Feeds
    • My Alert Summary & Preferences
  • News
    • Cancer Discovery News
    • Journal Press Releases
  • COVID-19
  • Webinars
  • 10th Anniversary
  • Search More

    Advanced Search

  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

User menu

  • Register
  • Log in
  • My Cart

Search

  • Advanced search
Cancer Discovery
Cancer Discovery
  • Home
  • About
    • The Journal
    • AACR Journals
    • Journal Sections
    • Subscriptions
    • Permissions and Reprints
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • Collections
      • COVID-19 & Cancer Resource Center
      • Precision Medicine and Therapeutic Resistance
      • Clinical Trials
      • Immuno-oncology
      • Editors' Picks
      • "Best of" Collection
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • Editors' Picks
    • OnlineFirst
    • Citation
    • Author/Keyword
    • RSS Feeds
    • My Alert Summary & Preferences
  • News
    • Cancer Discovery News
    • Journal Press Releases
  • COVID-19
  • Webinars
  • 10th Anniversary
  • Search More

    Advanced Search

In the Spotlight

Adipocytes and Neutrophils Give a Helping Hand to Pancreatic Cancers

Vincenzo Bronte and Giampaolo Tortora
Vincenzo Bronte
1Immunology, Department of Medicine, Verona University Hospital, Verona, Italy.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: vincenzo.bronte@univr.it
Giampaolo Tortora
2Medical Oncology, Department of Medicine, Verona University Hospital, Verona, Italy.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI: 10.1158/2159-8290.CD-16-0682 Published August 2016
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Abstract

Summary: Obesity-induced inflammation can build up a confined microenvironment in pancreatic adenocarcinoma that is associated with increased desmoplasia, neutrophil recruitment, reduced delivery of chemotherapeutic drugs, and immune evasion. Targeting molecular pathways empowering this circuit might represent a necessary measure to reach clinical efficacy for combination therapies in patients with excess body weight. Cancer Discov; 6(8); 821–3. ©2016 AACR.

See related article by Incio et al., p. 852.

Excess body weight amplifies the relative mortality risk in patients with pancreatic ductal adenocarcinoma (PDAC), a tumor characterized by a desmoplastic fibrotic reaction due to enhanced extracellular matrix deposition by activated pancreatic stellate cells (PSC). Moreover, pancreatic steatosis is associated with heightened PDAC risk and plays a negative prognostic role in patients with PDAC (1, 2). Starting from previously published data showing that obesity increases the proinflammatory cytokine IL1β and fuels an inflammatory milieu associated with accelerated tumor growth and metastasis formation, Incio and colleagues show that obesity shapes a distinctive PDAC microenvironment characterized by adipocyte accumulation and hypertrophy, local cross-talk between tumor-associated neutrophils (TAN) and PSCs, and the production of proinflammatory and profibrotic factors, which in turn favor tumor progression and severely limit the delivery of chemotherapeutic drugs (3). Some crucial molecular events support the intricate cell network that is established by diet-induced obesity. In invading the neighboring visceral white adipose tissue, whose adipocytes abundantly express the angiotensin II type-1 receptor (AT1), PDAC becomes enriched in enlarged adipocytes, collagen, and activated αSMA+ PSCs. This heightened desmoplastic context negatively affects blood perfusion and both delivery and therapeutic efficacy of the chemotherapeutic drug 5-Fluorouracil, one of the drugs commonly used in patients affected by PDAC. Such failure was reverted to that observed in lean mice by treatment with the FDA-approved AT1 inhibitor losartan or by AT1 genetic ablation (Agtr1a−/− mice; ref. 3). Obesity promoted TAN recruitment in PDAC, which in turn activated PSCs and limited vascular perfusion. Adipocytes and PSCs expressed high levels of IL1β that mediated the obesity-dependent TAN recruitment. Neutrophil depletion, IL1β inhibition, and AT1 blockade also increased CD8+ T cells and reduced T regulatory lymphocytes in tumors from obese but not lean mice, suggesting a role for TANs in regulating the immune contexture of PDAC. In line with the preclinical data, a study in 309 patients with PDAC confirmed that adjuvant chemotherapy following surgical resection resulted in a better overall survival in normal-weight patients compared with obese patients (3).

These data establish an important link between AT1+ adipocytes, IL1 production, neutrophil activation, and desmoplasia in pancreatic cancer (Fig. 1). IL1 family proteins comprise different cytokines with proinflammatory functions, often integrating endothelial activation and myeloid cell recruitment to optimize pathogen clearance. Among the members, IL1α and IL1β are produced, through different molecular mechanisms, by mesenchymal, epithelial, or myeloid cells but share the same receptor, and their chronic release has been associated with tumor promotion. In response to signals perturbing the mitogenic potential of tissue cells, including oncogenic insults, cells can mount a senescence response leading to a permanent cell-cycle arrest by tumor suppressors, such as p53 and p16INK4a, as well as the secretion of cytokines and proteases, a response termed the senescence-associated secretory phenotype (SASP). Cellular senescence is a potent anticancer mechanism in vitro, but SASP can puzzlingly create a protumorigenic environment in which IL1 plays an essential role. It is possible that this dichotomy is dictated by the interplay between the oncogenic and tissue landscape (Fig. 1), which include the presence and activation state of adipocytes, as supported by the original findings from Incio and colleagues (3). IL1α is produced, together with other inflammatory cytokines, by KRAS-induced senescent cells in mouse models of PDAC through the regulation of the histone-deacetylase-associate protein SIN3B. Genetic ablation of this gene delayed PDAC progression, and the levels of SIN3B in mouse and human PDAC correlated with KRAS-induced production of IL1α (4). Membrane-bound IL1α is the main SASP cytokine regulated by MTOR activation in senescent fibroblasts that can stimulate the growth of prostate cancer cells (5). CD11b+Gr1+ neutrophils recruited in mouse prostate tumors of PTEN-null mice, at the onset of senescence, protect proliferating cells and hence support tumor development. These TANs oppose IL1 activity within the tumor by releasing IL1 receptor antagonist, and the beneficial effect of senescence-activating chemotherapy with docetaxel was enhanced by interfering with TAN recruitment (6), further highlighting the multifaceted role of the IL1/neutrophil axis in cancer, at the beginning and later on during disease progression. Interestingly, a recent study demonstrated that KRASG12D mutation, common in the majority of PDACs, regulates not only tumor cell–autonomous signals but also nearby PSCs, which activate the IGF1/IGF1R and AKT axis, instigating reciprocal signaling on the tumor cells (7). Considering the role played by the IGF1/IGF1R axis in metabolism and fat storage, once again, the intricate interplay between PDAC cells and stroma is the clue to understanding the connection between obesity, inflammation, desmoplasia, and tumor progression in PDAC. Additionally, WNT5a-mediated signals can reprogram adipocytes toward fibroblast-like cells, which might profoundly influence the cancer microenvironment, when cocultured with PDAC cells (8). Cancer-intrinsic, oncogene-driven programs can thus variously affect adipocyte/PSC/neutrophil cross-talk, which in turn contributes to tumor development by molding a tumor-promoting stroma landscape (Fig. 1).

Figure 1.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure 1.

Cancer cell–intrinsic and –extrinsic cues to inflammation and fibrosis. Proinflammatory IL1 can be produced by either transformed cells or hijacked adipocytes to activate PSC, which can further amplify this loop by independent IL1 cytokine release. Recruited neutrophils establish extensive interactions with other cellular components of the stroma (i.e., adipocytes and PSC), creating a highly fibrotic and poorly vascularized tissue environment that is both refractory to free drug diffusion from blood and hostile to activation of tumor-specific CD8+ T cells. Treg, T regulatory lymphocyte.

The article by Incio and colleagues (3) also touches upon the immune-suppressive environment in PDAC, endorsing the IL1 role already proposed in other cancers. In mouse models of breast cancer dependent on mammary-restricted, combined loss of E-cadherin and p53, neutrophils facilitate metastatic spreading to different organs through a process initiated by tumor-released IL1β and amplified by the IL17 produced by γδ T lymphocytes and a systemic rise in G-CSF cytokine levels. In this cancer model, the tumor-promoting activity of neutrophils was dependent on the inhibitory action they exerted on metastasis-restraining CD8+ T cells (9). Even though IL1β or AT1 blockade resulted in concomitant TAN reduction and CD8+ T-cell increase in PDAC (3), suggesting an immune-suppressive role of obesity-induced neutrophils in limiting adaptive immunity (Fig. 1), a difference with the previous study in breast cancer lies in the observation that neutrophil depletion affected only metastasis formation and not the growth of primary tumor.

As suggested by Incio and colleagues, the different therapeutic options exploited to correct the tumor environment “poisoned” by the adipocyte infiltration in overweight patients might be exploited in combination with immunotherapy strategies reviving tumor-infiltrating CD8+ T cells, like the PD-1/PD-L1 checkpoint inhibitors. From this standpoint, however, it will be necessary to explore in depth the functional and responsive status of tumor-infiltrating CD8+ T cells in lean and obese mice to address whether obesity might either independently induce or aggravate some of the many immune regulatory circuits in cancer based on T-cell exhaustion and/or stroma-associated immunosuppression. This is also particularly relevant in consideration of the recent identification of four molecular subtypes of PDAC based on genes recurrently mutated in various signaling pathways (10). Considering the impact of different oncogenes on senescence and production of IL1 cytokine family members, obesity might exert diverse influences in distinctive subgroups of patients with PDAC.

The findings reported by Incio and colleagues (3) open two interesting scenarios, which will require further studies. The first is about the pervasiveness of the “adipocyte poisoning” of the tumor environment, i.e., whether this proinflammatory signature related to obesity can be present in other tumor types and determine specific features of tumor progression, such as fibrosis, immune dysfunction, angiogenesis, and senescence. The second and likely more clinically relevant point is related to the need of individualizing and optimizing combination therapies for obese patients by adding drugs targeting tumor-associated adipocytes.

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

Grant Support

V. Bronte is supported by grants from the Italian Ministry of Health (FINALIZZATA 2011-2012 RF-2011-02348435 cup: E35G1400019001); the Italian Association for Cancer Research (AIRC 6599, 12182, 14103); FP7-NMP-2011 (Trans-Int); EuroNanoMed II 2013 (NICHE); and the Fondazione Cassa di Risparmio di Verona, Vicenza, Belluno e Ancona. G. Tortora is supported by the Italian Association for Cancer Research (AIRC 12182, 12214).

  • ©2016 American Association for Cancer Research.

References

  1. 1.↵
    1. Hori M,
    2. Takahashi M,
    3. Hiraoka N,
    4. Yamaji T,
    5. Mutoh M,
    6. Ishigamori R,
    7. et al.
    Association of pancreatic Fatty infiltration with pancreatic ductal adenocarcinoma. Clin Transl Gastroenterol 2014;5:e53.
    OpenUrlCrossRef
  2. 2.↵
    1. Mathur A,
    2. Hernandez J,
    3. Shaheen F,
    4. Shroff M,
    5. Dahal S,
    6. Morton C,
    7. et al.
    Preoperative computed tomography measurements of pancreatic steatosis and visceral fat: prognostic markers for dissemination and lethality of pancreatic adenocarcinoma. HPB (Oxford) 2011;13:404–10.
    OpenUrlPubMed
  3. 3.↵
    1. Incio J,
    2. Liu H,
    3. Suboj P,
    4. Chin SM,
    5. Chen IX,
    6. Pinter M,
    7. et al.
    Obesity-induced inflammation and desmoplasia promote pancreatic cancer progression and resistance to chemotherapy. Cancer Discov 2016;6: 852–69.
  4. 4.↵
    1. Rielland M,
    2. Cantor DJ,
    3. Graveline R,
    4. Hajdu C,
    5. Mara L,
    6. Diaz Bde D,
    7. et al.
    Senescence-associated SIN3B promotes inflammation and pancreatic cancer progression. J Clin Invest 2014;124:2125–35.
    OpenUrlPubMed
  5. 5.↵
    1. Laberge RM,
    2. Sun Y,
    3. Orjalo AV,
    4. Patil CK,
    5. Freund A,
    6. Zhou L,
    7. et al.
    MTOR regulates the pro-tumorigenic senescence-associated secretory phenotype by promoting IL1A translation. Nat Cell Biol 2015;17:1049–61.
    OpenUrlCrossRefPubMed
  6. 6.↵
    1. Di Mitri D,
    2. Toso A,
    3. Chen JJ,
    4. Sarti M,
    5. Pinton S,
    6. Jost TR,
    7. et al.
    Tumour-infiltrating Gr-1+ myeloid cells antagonize senescence in cancer. Nature 2014;515:134–7.
    OpenUrlCrossRefPubMed
  7. 7.↵
    1. Tape CJ,
    2. Ling S,
    3. Dimitriadi M,
    4. McMahon KM,
    5. Worboys JD,
    6. Leong HS,
    7. et al.
    Oncogenic KRAS regulates tumor cell signaling via stromal reciprocation. Cell 2016;165:910–20.
    OpenUrlPubMed
  8. 8.↵
    1. Zoico E,
    2. Darra E,
    3. Rizzatti V,
    4. Budui S,
    5. Franceschetti G,
    6. Mazzali G,
    7. et al.
    Adipocytes Wnt5a mediated dedifferentiation: a possible target in pancreatic cancer microenvironment. Oncotarget 2016;7:20223–35.
    OpenUrlPubMed
  9. 9.↵
    1. Coffelt SB,
    2. Kersten K,
    3. Doornebal CW,
    4. Weiden J,
    5. Vrijland K,
    6. Hau CS,
    7. et al.
    IL-17-producing gammadelta T cells and neutrophils conspire to promote breast cancer metastasis. Nature 2015;522:345–8.
    OpenUrlCrossRefPubMed
  10. 10.↵
    1. Bailey P,
    2. Chang DK,
    3. Nones K,
    4. Johns AL,
    5. Patch AM,
    6. Gingras MC,
    7. et al.
    Genomic analyses identify molecular subtypes of pancreatic cancer. Nature 2016;531:47–52.
    OpenUrlCrossRefPubMed
PreviousNext
Back to top
Cancer Discovery: 6 (8)
August 2016
Volume 6, Issue 8
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover

Sign up for alerts

View this article with LENS

Open full page PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for sharing this Cancer Discovery article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Adipocytes and Neutrophils Give a Helping Hand to Pancreatic Cancers
(Your Name) has forwarded a page to you from Cancer Discovery
(Your Name) thought you would be interested in this article in Cancer Discovery.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Adipocytes and Neutrophils Give a Helping Hand to Pancreatic Cancers
Vincenzo Bronte and Giampaolo Tortora
Cancer Discov August 1 2016 (6) (8) 821-823; DOI: 10.1158/2159-8290.CD-16-0682

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Adipocytes and Neutrophils Give a Helping Hand to Pancreatic Cancers
Vincenzo Bronte and Giampaolo Tortora
Cancer Discov August 1 2016 (6) (8) 821-823; DOI: 10.1158/2159-8290.CD-16-0682
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Disclosure of Potential Conflicts of Interest
    • Grant Support
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
Advertisement

Related Articles

Cited By...

More in this TOC Section

  • At the Heart of Immune Checkpoint Inhibitor–Induced Immune Toxicity
  • Genetic Ancestry Correlations with Driver Mutations Suggest Complex Interactions between Somatic and Germline Variation in Cancer
  • Poorer Clinical Outcomes for Black Patients with AML: A Wake-Up Call for Better Data and Greater Understanding of Cancer Outcomes in All Ethnic Groups
Show more In the Spotlight
  • Home
  • Alerts
  • Feedback
  • Privacy Policy
Facebook   Twitter   LinkedIn   YouTube   RSS

Articles

  • OnlineFirst
  • Current Issue
  • Past Issues

Info For

  • Authors
  • Subscribers
  • Advertisers
  • Librarians

About Cancer Discovery

  • About the Journal
  • Editors
  • Journal Sections
  • Permissions
  • Submit a Manuscript
AACR logo

Copyright © 2021 by the American Association for Cancer Research.

Cancer Discovery
eISSN: 2159-8290
ISSN: 2159-8274

Advertisement