Cancer killers in the human gut microbiota: diverse phylogeny and broad spectra

Oncotarget. 2017 Jul 25;8(30):49574-49591. doi: 10.18632/oncotarget.17319.

Abstract

Cancer as a large group of complex diseases is believed to result from the interactions of numerous genetic and environmental factors but may develop in people without any known genetic or environmental risks, suggesting the existence of other powerful factors to influence the carcinogenesis process. Much attention has been focused recently on particular members of the intestinal microbiota for their potential roles in promoting carcinogenesis. Here we report the identification and characterization of intestinal bacteria that exhibited potent anti-malignancy activities on a broad range of solid cancers and leukemia. We collected fecal specimens from healthy individuals of different age groups (preschool children and university students), inspected their effects on cancer cells, and obtained bacteria with potent anti-malignancy activities. The bacteria mostly belonged to Actinobacteria but also included lineages of other phyla such as Proteobacteria and Firmicutes. In animal cancer models, sterile culture supernatant from the bacteria highly effectively inhibited tumor growth. Remarkably, intra-tumor administration of the bacterial products prevented metastasis and even cleared cancer cells at remote locations from the tumor site. This work demonstrates the prevalent existence of potent malignancy-killers in the human intestinal microbiota, which may routinely clear malignant cells from the body before they form cancers.

Keywords: Actinobacteria; cancer; gut microbiota; leukemia; malignancy killer.

MeSH terms

  • Adolescent
  • Adult
  • Animals
  • Bacteria / classification
  • Bacteria / genetics
  • Bacterial Physiological Phenomena
  • Cell Survival
  • Child
  • Child, Preschool
  • Disease Models, Animal
  • Feces / microbiology
  • Female
  • Gas Chromatography-Mass Spectrometry
  • Gastrointestinal Microbiome*
  • HeLa Cells
  • Humans
  • Male
  • Metagenome
  • Metagenomics / methods
  • Mice
  • Neoplasms / etiology*
  • Neoplasms / pathology
  • Phylogeny
  • RNA, Ribosomal, 16S / genetics
  • Young Adult

Substances

  • RNA, Ribosomal, 16S