Mammalian target of rapamycin inhibition after solid organ transplantation: can it, and does it, reduce cancer risk?

Clin Transplant. 2015 Jul;29(7):654-63. doi: 10.1111/ctr.12559. Epub 2015 Jun 10.

Abstract

The mammalian target of rapamycin (mTOR) inhibitors sirolimus and everolimus has been increasingly used as immunosuppressants for recipients of solid organ transplants. Over the years, potential advantages unique to this class of immunosuppressants have been recognized, including chemoprevention by virtue of their antiproliferative effects. Prevention of malignancy after transplant through mTOR inhibitor-based immunosuppression may have a specific practical application in transplant recipients with preexisting malignancy including hepatocellular carcinoma or cholangiocarcinoma. This review will reveal how the biochemistry of the mTOR pathway, as it pertains to chemoprevention, can support a clinical role for mTOR inhibitors in the prevention of malignancies, recurrent or de novo, after solid organ transplantation in selected patients.

Keywords: everolimus; immunosuppression; malignancy; mammalian target of rapamycin inhibitor; sirolimus; transplant.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Graft Rejection / etiology
  • Graft Rejection / prevention & control*
  • Graft Survival
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Neoplasms / etiology
  • Neoplasms / prevention & control*
  • Organ Transplantation*
  • Postoperative Complications*
  • Prognosis
  • Risk Factors
  • TOR Serine-Threonine Kinases / antagonists & inhibitors*

Substances

  • Immunosuppressive Agents
  • MTOR protein, human
  • TOR Serine-Threonine Kinases