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Sökning: onr:"swepub:oai:gup.ub.gu.se/294838" > LGR5 in breast canc...

LGR5 in breast cancer and ductal carcinoma in situ: a diagnostic and prognostic biomarker and a therapeutic target

Hagerling, Catharina (författare)
Lund University,Lunds universitet,Cancercellers evolution,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Pathways of cancer cell evolution,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments,UCSF Helen Diller Family Comprehensive Cancer Center,University of California, San Francisco
Owyong, M. (författare)
University of California, San Francisco,UCSF Helen Diller Family Comprehensive Cancer Center
Sitarama, V. (författare)
UCSF Helen Diller Family Comprehensive Cancer Center,University of California, San Francisco
visa fler...
Wang, C. Y. (författare)
National Cheng Kung University,UCSF Helen Diller Family Comprehensive Cancer Center,University of California, San Francisco
Lin, C. (författare)
University of California, San Francisco,UCSF Helen Diller Family Comprehensive Cancer Center
van den Bijgaart, R. J. E. (författare)
UCSF Helen Diller Family Comprehensive Cancer Center,Radboud University Medical Center,University of California, San Francisco
Koopman, C. D. (författare)
University of California, San Francisco,University Medical Center Utrecht,UCSF Helen Diller Family Comprehensive Cancer Center
Brenot, A. (författare)
Washington University in St. Louis,University of California, San Francisco,UCSF Helen Diller Family Comprehensive Cancer Center
Nanjaraj, A. (författare)
University of California, San Francisco,UCSF Helen Diller Family Comprehensive Cancer Center
Wärnberg, Fredrik (författare)
University of Gothenburg,Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för kirurgi,Institute of Clinical Sciences, Department of Surgery,Sahlgrenska University Hospital
Jirström, Karin (författare)
Lund University,Lunds universitet,Terapeutisk patologi,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Therapeutic pathology,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,LUCC: Lund University Cancer Centre,Other Strong Research Environments
Klein, O. D. (författare)
University of California, San Francisco
Werb, Z. (författare)
UCSF Helen Diller Family Comprehensive Cancer Center,University of California, San Francisco
Plaks, V. (författare)
UCSF Helen Diller Family Comprehensive Cancer Center,University of California, San Francisco
visa färre...
 (creator_code:org_t)
2020-06-10
2020
Engelska.
Ingår i: Bmc Cancer. - : Springer Science and Business Media LLC. - 1471-2407. ; 20:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background Novel biomarkers are required to discern between breast tumors that should be targeted for treatment from those that would never become clinically apparent and/or life threatening for patients. Moreover, therapeutics that specifically target breast cancer (BC) cells with tumor-initiating capacity to prevent recurrence are an unmet need. We investigated the clinical importance of LGR5 in BC and ductal carcinoma in situ (DCIS) to explore LGR5 as a biomarker and a therapeutic target. Methods We stained BC (n = 401) and DCIS (n = 119) tissue microarrays with an antibody against LGR5. We examined anLGR5knockdown ER(-)cell line that was orthotopically transplanted and used for in vitro colony assays. We also determined the tumor-initiating role of Lgr5 in lineage-tracing experiments. Lastly, we transplanted ER(-)patient-derived xenografts into mice that were subsequently treated with a LGR5 antibody drug conjugate (anti-LGR5-ADC). Results LGR5 expression correlated with small tumor size, lower grade, lymph node negativity, and ER-positivity. ER(+)patients with LGR5(high)tumors rarely had recurrence, while high-grade ER(-)patients with LGR5(high)expression recurred and died due to BC more often. Intriguingly, all the DCIS patients who later died of BC had LGR5-positive tumors. Colony assays and xenograft experiments substantiated a role for LGR5 in ER(-)tumor initiation and subsequent growth, which was further validated by lineage-tracing experiments in ER-/triple-negative BC mouse models. Importantly, by utilizing LGR5(high)patient-derived xenografts, we showed that anti-LGR5-ADC should be considered as a therapeutic for high-grade ER-BC. Conclusion LGR5 has distinct roles in ER(-)vs. ER+BC with potential clinical applicability as a biomarker to identify patients in need of therapy and could serve as a therapeutic target for high-grade ER-BC.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

LGR5
Breast cancer
DCIS
Estrogen receptor
Targeted therapy
mammary stem-cells
genomic differences
small-intestine
self-renewal
progression
identification
marker
overdiagnosis
overtreatment
mammography
Oncology

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