SwePub
Sök i LIBRIS databas

  Utökad sökning

onr:"swepub:oai:DiVA.org:uu-377673"
 

Sökning: onr:"swepub:oai:DiVA.org:uu-377673" > Protein profiling o...

Protein profiling of fine-needle aspirates reveals subtype-associated immune signatures and involvement of chemokines in breast cancer

Franzen, Bo (författare)
Karolinska Institutet
Alexeyenko, Andrey (författare)
Karolinska Institutet
Kamali-Moghaddam, Masood (författare)
Uppsala universitet,Molekylära verktyg,Science for Life Laboratory, SciLifeLab
visa fler...
Hatschek, Thomas (författare)
Karolinska Institutet
Kanter, Lena (författare)
Karolinska Institutet
Ramqvist, Torbjorn (författare)
Karolinska Institutet
Kierkegaard, Jonas (författare)
BrostCtr City, Stockholm, Sweden;Capio St Gorans Sjukhus, Stockholm, Sweden
Masucci, Giuseppe (författare)
Karolinska Institutet
Auer, Gert (författare)
Karolinska Institutet
Landegren, Ulf (författare)
Uppsala universitet,Molekylära verktyg,Science for Life Laboratory, SciLifeLab
Lewensohn, Rolf (författare)
Karolinska Institutet
visa färre...
 (creator_code:org_t)
2019-01-07
2019
Engelska.
Ingår i: Molecular Oncology. - : WILEY. - 1574-7891 .- 1878-0261. ; 13:2, s. 376-391
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • There are increasing demands for informative cancer biomarkers, accessible via minimally invasive procedures, both for initial diagnostics and for follow-up of personalized cancer therapy, including immunotherapy. Fine-needle aspiration (FNA) biopsy provides ready access to relevant tissue samples; however, the minute amounts of sample require sensitive multiplex molecular analysis to be of clinical biomarker utility. We have applied proximity extension assays (PEA) to analyze 167 proteins in FNA samples from patients with breast cancer (BC; n = 25) and benign lesions (n = 32). We demonstrate that the FNA BC samples could be divided into two main clusters, characterized by differences in expression levels of the estrogen receptor (ER) and the proliferation marker Ki67. This clustering corresponded to some extent to established BC subtypes. Our analysis also revealed several proteins whose expression levels differed between BC and benign lesions (e.g., CA9, GZMB, IL-6, VEGFA, CXCL11, PDL1, and PCD1), as well as several chemokines correlating with ER and Ki67 status (e.g., CCL4, CCL8, CCL20, CXCL8, CXCL9, and CXCL17). Finally, we also identified three signatures that could predict Ki67 status, ER status, and tumor grade, respectively, based on a small subset of proteins, which was dominated by chemokines. To our knowledge, expression profiles of CCL13 in benign lesions and BC have not previously been described but were shown herein to correlate with proliferation (P = 0.00095), suggesting a role in advanced BC. Given the broad functional range of the proteins analyzed, immune-related proteins were overrepresented among the observed alterations. Our pilot study supports the emerging role of chemokines in BC progression. Due to the minimally traumatic sampling and clinically important molecular information for therapeutic decisions, this methodology is promising for future immunoscoring and monitoring of treatment efficacy in BC.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Nyckelord

breast cancer subtypes
fibroadenomas
fine-needle aspiration
immune-related protein biomarker
proximity extension assay

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy