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A drug screening assay on cancer cells chronically adapted to acidosis

Pellegrini, Paola (författare)
Karolinska Institutet,Karolinska Inst, Sweden
Serviss, Jason T. (författare)
Karolinska Institutet,Karolinska Inst, Sweden
Lundback, Thomas (författare)
Karolinska Institutet,Chem Biol Consortium Sweden, Sweden; AstraZeneca, Sweden
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Bancaro, Nicolo (författare)
Karolinska Inst, Sweden
Mazurkiewicz, Magdalena (författare)
Karolinska Institutet,Karolinska Inst, Sweden
Kolosenko, Iryna (författare)
Karolinska Inst, Sweden
Yu, Di (författare)
Karolinska Inst, Sweden
Haraldsson, Martin (författare)
Chem Biol Consortium Sweden, Sweden
D´arcy, Padraig (författare)
Linköpings universitet,Avdelningen för läkemedelsforskning,Medicinska fakulteten
Linder, Stig (författare)
Karolinska Institutet,Linköpings universitet,Avdelningen för läkemedelsforskning,Medicinska fakulteten
De Milito, Angelo (författare)
Karolinska Institutet,Karolinska Inst, Sweden
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 (creator_code:org_t)
2018-09-25
2018
Engelska.
Ingår i: Cancer Cell International. - : BMC. - 1475-2867. ; 18
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: Drug screening for the identification of compounds with anticancer activity is commonly performed using cell lines cultured under normal oxygen pressure and physiological pH. However, solid tumors are characterized by a microenvironment with limited access to nutrients, reduced oxygen supply and acidosis. Tumor hypoxia and acidosis have been identified as important drivers of malignant progression and contribute to multicellular resistance to different forms of therapy. Tumor acidosis represents an important mechanism mediating drug resistance thus the identification of drugs active on acid-adapted cells may improve the efficacy of cancer therapy. Methods: Here, we characterized human colon carcinoma cells (HCT116) chronically adapted to grow at pH 6.8 and used them to screen the Prestwick drug library for cytotoxic compounds. Analysis of gene expression profiles in parental and low pH-adapted cells showed several differences relating to cell cycle, metabolism and autophagy. Results: The screen led to the identification of several compounds which were further selected for their preferential cytotoxicity towards acid-adapted cells. Amongst 11 confirmed hits, we primarily focused our investigation on the benzoporphyrin derivative Verteporfin (VP). VP significantly reduced viability in low pH-adapted HCT116 cells as compared to parental HCT116 cells and normal immortalized epithelial cells. The cytotoxic activity of VP was enhanced by light activation and acidic pH culture conditions, likely via increased acid-dependent drug uptake. VP displayed the unique property to cause light-dependent cross-linking of proteins and resulted in accumulation of polyubiquitinated proteins without inducing inhibition of the proteasome. Conclusions: Our study provides an example and a tool to identify anticancer drugs targeting acid-adapted cancer cells.

Ämnesord

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

Nyckelord

Tumor acidosis; Drug resistance; RNAseq; Verteporfin; Drug screening

Publikations- och innehållstyp

ref (ämneskategori)
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