Several molecular and cellular markers are currently used as prognostic indicators for diagnosis and
therapeutic intervention of breast cancer. Although some of these markers have helped clinicians provide an
earlier diagnosis (or prognosis), they have failed to provide adequate information about the mechanisms
responsible for different stages of tumor malignancy so that more effective anticancer therapies can be
developed. Recently translocator protein (TSPO), formerly known as the peripheral benzodiazepine receptor
(PBR), has received attention as a potential target for anticancer drug development. It is a well-conserved
protein, located at outer-inner mitochondrial membrane contact sites, and is expressed in almost all tissues,
although the level of expression varies. TSPO is closely associated with the 32 kDa voltage-dependent anion
channel (VDAC) and the 30 kDa adenine nucleotide translocase (ANT), considered to form the core of a
mitochondria multiprotein complex [named the mitochondrial permeability transition pore (MPTP)] and plays a
role in apoptotic cell death. As the major role of TSPO is steroid biosynthesis, TSPO expression is particularly
high in organs involved in steroidogenesis such as the adrenals, testes, ovaries, placenta, prostate, colon,
kidney, and cardiovascular system. It is well known that TSPO is over-expressed in highly aggressive tumors,
especially those of the breast, and that expression correlates with advancing stages of this malignancy. TSPO
expression, nuclear localization, and TSPO-mediated cholesterol transport into the nucleus are involved in
breast cancer cell proliferation and aggressive phenotype expression. Hence, it can be used as a biomarker in
the stage-dependent diagnosis of this cancer.
In addition, cell proliferation, invasion and migration appears to be decreased when treated with high doses of
TSPO ligand PK-11195, a compound that may represent a therapeutic agent for the control of breast cancer
progression. Control of breast cancer development by consumption of dietary soy protein has been linked to
down-regulation of the expression of TSPO-mediated angiogenic signaling molecules. This chapter provides
insight into the potential of TSPO as a rational target for the development of novel therapeutics for breast
cancer.