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Catabolism of exogenous lactate reveals it as a legitimate metabolic substrate in breast cancer.

Publication ,  Journal Article
Kennedy, KM; Scarbrough, PM; Ribeiro, A; Richardson, R; Yuan, H; Sonveaux, P; Landon, CD; Chi, J-T; Pizzo, S; Schroeder, T; Dewhirst, MW
Published in: PLoS One
2013

Lactate accumulation in tumors has been associated with metastases and poor overall survival in cancer patients. Lactate promotes angiogenesis and metastasis, providing rationale for understanding how it is processed by cells. The concentration of lactate in tumors is a balance between the amount produced, amount carried away by vasculature and if/how it is catabolized by aerobic tumor or stromal cells. We examined lactate metabolism in human normal and breast tumor cell lines and rat breast cancer: 1. at relevant concentrations, 2. under aerobic vs. hypoxic conditions, 3. under conditions of normo vs. hypoglucosis. We also compared the avidity of tumors for lactate vs. glucose and identified key lactate catabolites to reveal how breast cancer cells process it. Lactate was non-toxic at clinically relevant concentrations. It was taken up and catabolized to alanine and glutamate by all cell lines. Kinetic uptake rates of lactate in vivo surpassed that of glucose in R3230Ac mammary carcinomas. The uptake appeared specific to aerobic tumor regions, consistent with the proposed "metabolic symbiont" model; here lactate produced by hypoxic cells is used by aerobic cells. We investigated whether treatment with alpha-cyano-4-hydroxycinnamate (CHC), a MCT1 inhibitor, would kill cells in the presence of high lactate. Both 0.1 mM and 5 mM CHC prevented lactate uptake in R3230Ac cells at lactate concentrations at ≤ 20 mM but not at 40 mM. 0.1 mM CHC was well-tolerated by R3230Ac and MCF7 cells, but 5 mM CHC killed both cell lines ± lactate, indicating off-target effects. This study showed that breast cancer cells tolerate and use lactate at clinically relevant concentrations in vitro (± glucose) and in vivo. We provided additional support for the metabolic symbiont model and discovered that breast cells prevailingly take up and catabolize lactate, providing rationale for future studies on manipulation of lactate catabolism pathways for therapy.

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Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2013

Volume

8

Issue

9

Start / End Page

e75154

Location

United States

Related Subject Headings

  • Rats
  • Neoplasm Staging
  • Middle Aged
  • Metabolomics
  • Metabolic Networks and Pathways
  • Lactic Acid
  • Kinetics
  • Humans
  • Glutamic Acid
  • Glucose
 

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Kennedy, K. M., Scarbrough, P. M., Ribeiro, A., Richardson, R., Yuan, H., Sonveaux, P., … Dewhirst, M. W. (2013). Catabolism of exogenous lactate reveals it as a legitimate metabolic substrate in breast cancer. PLoS One, 8(9), e75154. https://doi.org/10.1371/journal.pone.0075154
Kennedy, Kelly M., Peter M. Scarbrough, Anthony Ribeiro, Rachel Richardson, Hong Yuan, Pierre Sonveaux, Chelsea D. Landon, et al. “Catabolism of exogenous lactate reveals it as a legitimate metabolic substrate in breast cancer.PLoS One 8, no. 9 (2013): e75154. https://doi.org/10.1371/journal.pone.0075154.
Kennedy KM, Scarbrough PM, Ribeiro A, Richardson R, Yuan H, Sonveaux P, et al. Catabolism of exogenous lactate reveals it as a legitimate metabolic substrate in breast cancer. PLoS One. 2013;8(9):e75154.
Kennedy, Kelly M., et al. “Catabolism of exogenous lactate reveals it as a legitimate metabolic substrate in breast cancer.PLoS One, vol. 8, no. 9, 2013, p. e75154. Pubmed, doi:10.1371/journal.pone.0075154.
Kennedy KM, Scarbrough PM, Ribeiro A, Richardson R, Yuan H, Sonveaux P, Landon CD, Chi J-T, Pizzo S, Schroeder T, Dewhirst MW. Catabolism of exogenous lactate reveals it as a legitimate metabolic substrate in breast cancer. PLoS One. 2013;8(9):e75154.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2013

Volume

8

Issue

9

Start / End Page

e75154

Location

United States

Related Subject Headings

  • Rats
  • Neoplasm Staging
  • Middle Aged
  • Metabolomics
  • Metabolic Networks and Pathways
  • Lactic Acid
  • Kinetics
  • Humans
  • Glutamic Acid
  • Glucose