IR-783 inhibits breast cancer cell proliferation and migration by inducing mitochondrial fission

Pantong Li1, Yu Liu1, Wuyi Liu2

  • 1Department of Pharmacy, The University-Town Hospital of Chongqing Medical University, Chongqing 401331, P.R. China.

Insights

IR-783, a near-infrared dye, effectively inhibits breast cancer cell proliferation and migration. It works by inducing mitochondrial fission, reducing ATP levels, and causing cell cycle arrest, suggesting its potential as a novel breast cancer therapeutic.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • IR-783, a near-infrared heptamethine cyanine dye, shows promise for cancer targeting and treatment.
  • The precise molecular mechanisms underlying IR-783's anti-breast cancer effects remain largely unelucidated.

Purpose of the Study:

  • To investigate the inhibitory effects of IR-783 on breast cancer cell proliferation and migration.
  • To elucidate the molecular mechanisms responsible for IR-783's anti-breast cancer activity.

Main Methods:

  • Cell proliferation assays were performed on MDA-MB-231 and MCF-7 cell lines.
  • Cell migration was assessed using Transwell assays.
  • Mitochondrial function, ATP levels, and actin polymerization were analyzed post-IR-783 treatment.

Main Results:

  • IR-783 demonstrated dose- and time-dependent inhibition of MDA-MB-231 and MCF-7 cell proliferation by inducing G0/G1 cell cycle arrest.
  • IR-783 significantly suppressed the migratory capacity of both cell lines and reduced matrix metalloproteinase (MMP)-2 and MMP-9 expression in MDA-MB-231 cells.
  • IR-783 induced mitochondrial fission, decreased ATP levels, and reduced polymerized filamentous actin, inhibiting filopodia formation.

Conclusions:

  • IR-783 inhibits breast cancer cell proliferation and migration through mitochondrial fission and subsequent ATP depletion, leading to cell cycle arrest and suppressed filopodia formation.
  • These findings highlight IR-783 as a potential novel therapeutic agent for breast cancer treatment.

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