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Fibrinogen-like protein 2 in gastrointestinal stromal tumour

Pulkka, Olli Pekka (author)
University of Helsinki
Viisanen, Leevi (author)
University of Helsinki
Tynninen, Olli (author)
Helsinki University Central Hospital
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Laaksonen, Maria (author)
Reichardt, Peter (author)
HELIOS Klinikum Berlin-Buch
Reichardt, Annette (author)
HELIOS Klinikum Berlin-Buch
Eriksson, Mikael (author)
Lund University,Lunds universitet,Medicinsk onkologi,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Medical oncology,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,LUCC: Lund University Cancer Centre,Other Strong Research Environments,Skåne University Hospital
Hall, Kirsten Sundby (author)
Norwegian Radium Hospital
Wardelmann, Eva (author)
University Hospital Münster
Nilsson, Bengt (author)
Sahlgrenska University Hospital
Sihto, Harri (author)
University of Helsinki
Joensuu, Heikki (author)
University of Helsinki,Helsinki University Central Hospital
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 (creator_code:org_t)
2022-01-14
2022
English.
In: Journal of Cellular and Molecular Medicine. - : Wiley. - 1582-1838 .- 1582-4934. ; 26:4, s. 1083-1094
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Gastrointestinal stromal tumour (GIST), the most common sarcoma of the gastrointestinal tract, can be treated effectively with tyrosine kinase inhibitors, such as imatinib. Cancer immune therapy has limited efficacy, and little is known about the immune suppressive factors in GISTs. Fibrinogen-like protein 2 (FGL2) is expressed either as a membrane-associated protein or as a secreted soluble protein that has immune suppressive functions. We found that GISTs expressed FGL2 mRNA highly compared to other types of cancer in a large human cancer transcriptome database. GIST expressed FGL2 frequently also when studied using immunohistochemistry in two large clinical series, where 333 (78%) out of the 425 GISTs were FGL2 positive. The interstitial cells of Cajal, from which GISTs may originate, expressed FGL2. FGL2 expression was associated with small GIST size, low mitotic counts and low tumour-infiltrating lymphocyte (TIL) counts. Patients whose GIST expressed FGL2 had better recurrence-free survival than patients whose GIST lacked expression. Imatinib upregulated FGL2 in GIST cell lines, and the patients with FGL2-negative GIST appeared to benefit most from long duration of adjuvant imatinib. We conclude that GISTs express FGL2 frequently and that FGL2 expression is associated with low TIL counts and favourable survival outcomes.

Subject headings

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

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