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Targeting LIF-mediated paracrine interaction for pancreatic cancer therapy and monitoring.

Publication ,  Journal Article
Shi, Y; Gao, W; Lytle, NK; Huang, P; Yuan, X; Dann, AM; Ridinger-Saison, M; DelGiorno, KE; Antal, CE; Liang, G; Atkins, AR; Erikson, G; Xu, R ...
Published in: Nature
May 2019

Pancreatic ductal adenocarcinoma (PDAC) has a dismal prognosis largely owing to inefficient diagnosis and tenacious drug resistance. Activation of pancreatic stellate cells (PSCs) and consequent development of dense stroma are prominent features accounting for this aggressive biology1,2. The reciprocal interplay between PSCs and pancreatic cancer cells (PCCs) not only enhances tumour progression and metastasis but also sustains their own activation, facilitating a vicious cycle to exacerbate tumorigenesis and drug resistance3-7. Furthermore, PSC activation occurs very early during PDAC tumorigenesis8-10, and activated PSCs comprise a substantial fraction of the tumour mass, providing a rich source of readily detectable factors. Therefore, we hypothesized that the communication between PSCs and PCCs could be an exploitable target to develop effective strategies for PDAC therapy and diagnosis. Here, starting with a systematic proteomic investigation of secreted disease mediators and underlying molecular mechanisms, we reveal that leukaemia inhibitory factor (LIF) is a key paracrine factor from activated PSCs acting on cancer cells. Both pharmacologic LIF blockade and genetic Lifr deletion markedly slow tumour progression and augment the efficacy of chemotherapy to prolong survival of PDAC mouse models, mainly by modulating cancer cell differentiation and epithelial-mesenchymal transition status. Moreover, in both mouse models and human PDAC, aberrant production of LIF in the pancreas is restricted to pathological conditions and correlates with PDAC pathogenesis, and changes in the levels of circulating LIF correlate well with tumour response to therapy. Collectively, these findings reveal a function of LIF in PDAC tumorigenesis, and suggest its translational potential as an attractive therapeutic target and circulating marker. Our studies underscore how a better understanding of cell-cell communication within the tumour microenvironment can suggest novel strategies for cancer therapy.

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Published In

Nature

DOI

EISSN

1476-4687

ISSN

0028-0836

Publication Date

May 2019

Volume

569

Issue

7754

Start / End Page

131 / 135

Related Subject Headings

  • Tumor Microenvironment
  • Receptors, OSM-LIF
  • Paracrine Communication
  • Pancreatic Neoplasms
  • Mice
  • Mass Spectrometry
  • Male
  • Leukemia Inhibitory Factor
  • Humans
  • General Science & Technology
 

Citation

APA
Chicago
ICMJE
MLA
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Shi, Y., Gao, W., Lytle, N. K., Huang, P., Yuan, X., Dann, A. M., … Hunter, T. (2019). Targeting LIF-mediated paracrine interaction for pancreatic cancer therapy and monitoring. Nature, 569(7754), 131–135. https://doi.org/10.1038/s41586-019-1130-6
Shi, Yu, Weina Gao, Nikki K. Lytle, Peiwu Huang, Xiao Yuan, Amanda M. Dann, Maya Ridinger-Saison, et al. “Targeting LIF-mediated paracrine interaction for pancreatic cancer therapy and monitoring.Nature 569, no. 7754 (May 2019): 131–35. https://doi.org/10.1038/s41586-019-1130-6.
Shi Y, Gao W, Lytle NK, Huang P, Yuan X, Dann AM, et al. Targeting LIF-mediated paracrine interaction for pancreatic cancer therapy and monitoring. Nature. 2019 May;569(7754):131–5.
Shi, Yu, et al. “Targeting LIF-mediated paracrine interaction for pancreatic cancer therapy and monitoring.Nature, vol. 569, no. 7754, May 2019, pp. 131–35. Epmc, doi:10.1038/s41586-019-1130-6.
Shi Y, Gao W, Lytle NK, Huang P, Yuan X, Dann AM, Ridinger-Saison M, DelGiorno KE, Antal CE, Liang G, Atkins AR, Erikson G, Sun H, Meisenhelder J, Terenziani E, Woo G, Fang L, Santisakultarm TP, Manor U, Xu R, Becerra CR, Borazanci E, Von Hoff DD, Grandgenett PM, Hollingsworth MA, Leblanc M, Umetsu SE, Collisson EA, Scadeng M, Lowy AM, Donahue TR, Reya T, Downes M, Evans RM, Wahl GM, Pawson T, Tian R, Hunter T. Targeting LIF-mediated paracrine interaction for pancreatic cancer therapy and monitoring. Nature. 2019 May;569(7754):131–135.
Journal cover image

Published In

Nature

DOI

EISSN

1476-4687

ISSN

0028-0836

Publication Date

May 2019

Volume

569

Issue

7754

Start / End Page

131 / 135

Related Subject Headings

  • Tumor Microenvironment
  • Receptors, OSM-LIF
  • Paracrine Communication
  • Pancreatic Neoplasms
  • Mice
  • Mass Spectrometry
  • Male
  • Leukemia Inhibitory Factor
  • Humans
  • General Science & Technology