Is there an effect of ghrelin/ghrelin analogs on cancer? A systematic review

Endocr Relat Cancer. 2016 Sep;23(9):R393-409. doi: 10.1530/ERC-16-0130.

Abstract

Ghrelin is a hormone with multiple physiologic functions, including promotion of growth hormone release, stimulation of appetite and regulation of energy homeostasis. Treatment with ghrelin/ghrelin-receptor agonists is a prospective therapy for disease-related cachexia and malnutrition. In vitro studies have shown high expression of ghrelin in cancer tissue, although its role including its impact in cancer risk and progression has not been established. We performed a systematic literature review to identify peer-reviewed human or animal in vivo original research studies of ghrelin, ghrelin-receptor agonists, or ghrelin genetic variants and the risk, presence, or growth of cancer using structured searches in PubMed database as well as secondary searches of article reference lists, additional reviews and meta-analyses. Overall, 45 (73.8%) of the 61 studies reviewed, including all 11 involving exogenous ghrelin/ghrelin-receptor agonist treatment, reported either a null (no statistically significant difference) or inverse association of ghrelin/ghrelin-receptor agonists or ghrelin genetic variants with cancer risk, presence or growth; 10 (16.7%) studies reported positive associations; and 6 (10.0%) reported both negative or null and positive associations. Differences in serum ghrelin levels in cancer cases vs controls (typically lower) were reported for some but not all cancers. The majority of in vivo studies showed a null or inverse association of ghrelin with risk and progression of most cancers, suggesting that ghrelin/ghrelin-receptor agonist treatment may have a favorable safety profile to use for cancer cachexia. Additional large-scale prospective clinical trials as well as basic bioscientific research are warranted to further evaluate the safety and benefits of ghrelin treatment in patients with cancer.

Keywords: cachexia; cancer; ghrelin; in vivo; metastasis; tumor growth.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Animals
  • Ghrelin* / analogs & derivatives
  • Ghrelin* / blood
  • Ghrelin* / genetics
  • Ghrelin* / therapeutic use
  • Humans
  • Neoplasms* / blood
  • Neoplasms* / drug therapy
  • Neoplasms* / genetics
  • Receptors, Ghrelin / agonists*

Substances

  • Ghrelin
  • Receptors, Ghrelin