Extracellular Acidification Induces Lysosomal Dysregulation

Cells. 2021 May 13;10(5):1188. doi: 10.3390/cells10051188.

Abstract

Many invasive cancers emerge through a years-long process of somatic evolution, characterized by an accumulation of heritable genetic and epigenetic changes and the emergence of increasingly aggressive clonal populations. In solid tumors, such as breast ductal carcinoma, the extracellular environment for cells within the nascent tumor is harsh and imposes different types of stress on cells, such as hypoxia, nutrient deprivation, and cytokine inflammation. Acidosis is a constant stressor of most cancer cells due to its production through fermentation of glucose to lactic acid in hypoxic or normoxic regions (Warburg effect). Over a short period of time, acid stress can have a profound effect on the function of lysosomes within the cells exposed to this environment, and after long term exposure, lysosomal function of the cancer cells can become completely dysregulated. Whether this dysregulation is due to an epigenetic change or evolutionary selection has yet to be determined, but understanding the mechanisms behind this dysregulation could identify therapeutic opportunities.

Keywords: Warburg effect; breast cancer; cancer acidosis; cancer metastasis; intracellular pH; lysosomal localization; lysosome dysregulation; targeted therapy; tumor microenvironment.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Acidosis / drug therapy
  • Acidosis / genetics
  • Acidosis / metabolism*
  • Acidosis / pathology
  • Animals
  • Antineoplastic Agents / therapeutic use
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Carcinoma, Ductal, Breast / drug therapy
  • Carcinoma, Ductal, Breast / genetics
  • Carcinoma, Ductal, Breast / metabolism*
  • Carcinoma, Ductal, Breast / pathology
  • Energy Metabolism
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Lysosomes / drug effects
  • Lysosomes / metabolism*
  • Lysosomes / pathology
  • Molecular Targeted Therapy
  • Tumor Microenvironment*
  • Warburg Effect, Oncologic

Substances

  • Antineoplastic Agents