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Novel activity of acriflavine against colorectal cancer tumor cells

Hassan, Saadia (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics/Rolf Larsson
Laryea, Daniel (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics/Rolf Larsson
Mahteme, Haile (author)
Uppsala universitet,Kolorektalkirurgi
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Felth, Jenny (author)
Uppsala universitet,Avdelningen för farmakognosi
Fryknäs, Mårten (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics/Rolf Larsson
Fayad, Walid (author)
Oncology and pathology - Karolinska Institutet
Linder, Stig (author)
Karolinska Institutet
Rickardson, Linda (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics/Rolf Larsson
Gullbo, Joachim (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics/Rolf Larsson
Graf, Wilhelm (author)
Uppsala universitet,Kolorektalkirurgi
Pålman, Lars (author)
Uppsala universitet,Kolorektalkirurgi
Glimelius, Bengt (author)
Uppsala universitet,Enheten för onkologi
Larsson, Rolf (author)
Uppsala universitet,Klinisk farmakologi,Cancer Pharmacology and Informatics/Rolf Larsson
Nygren, Peter (author)
Uppsala universitet,Enheten för onkologi,Nygren
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 (creator_code:org_t)
2011-10-12
2011
English.
In: Cancer Science. - : Wiley. - 1347-9032 .- 1349-7006. ; 102:12, s. 2206-2213
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A high-throughput screen of the cytotoxic activity of 2000 molecules from a commercial library in three human colon cancer cell lines and two normal cell types identified the acridine acriflavin to be a colorectal cancer (CRC) active drug. Acriflavine was active in cell spheroids, indicating good drug penetration and activity against hypoxic cells. In a validation step based on primary cultures of patient tumor cells, acriflavine was found to be more active against CRC than ovarian cancer and chronic lymphocytic leukemia. This contrasted to the activity pattern of the CRC active standard drugs 5-fluorouracil, irinotecan and oxaliplatin. Mechanistic studies indicated acriflavine to be a dual topoisomerase I and II inhibitor. In conclusion, the strategy used seems promising for identification of new diagnosis-specific cancer drugs.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

Acriflavine
colorectal cancer
topoisomerase
drug screening
Clinical pharmacology
Klinisk farmakologi
Medicin
Medicine

Publication and Content Type

ref (subject category)
art (subject category)

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