The palladacycle, BTC2, exhibits anti-breast cancer and breast cancer stem cell activity

Biochem Pharmacol. 2021 Aug:190:114598. doi: 10.1016/j.bcp.2021.114598. Epub 2021 May 9.

Abstract

In women globally, breast cancer is responsible for most cancer-related deaths and thus, new effective therapeutic strategies are required to treat this malignancy. Platinum-based compounds like cisplatin are widely used to treat breast cancer, however, they come with limitations such as poor solubility, adverse effects, and drug resistance. To overcome these limitations, complexes containing other platinum group metals such as palladium have been studied and some have already entered clinical trials. Here we investigated the anti-cancer activity of a palladium complex, BTC2, in MCF-7 oestrogen receptor positive (ER+) and MDA-MB-231 triple negative (TN) human breast cancer cells as well as in a human breast cancer xenograft chick embryo model. BTC2 exhibited an average IC50 value of 0.54 μM, a desirable selectivity index of >2, inhibited the migration of ER+ and TN breast cancer cells, and displayed anti-cancer stem cell activity. We demonstrate that BTC2 induced DNA double strand breaks (increased levels of γ-H2AX) and activated the p-ATM/p-CHK2 and p-p38/MAPK pathways resulting in S- and G2/M-phase cell cycle arrests. Importantly, BTC2 sensitised breast cancer cells by triggering the intrinsic (cleaved caspase 9) and extrinsic (cleaved caspase 8) apoptotic as well as necroptotic (p-RIP3 and p-MLKL) cell death pathways and inhibiting autophagy and its pro-survival role. Furthermore, in the xenograft in vivo model, BTC2 displayed limited toxicity and arrested the tumour growth of breast cancer cells over a 9-day period in a manner comparable to that of the positive control drug, paclitaxel. BTC2 thus displayed promising anti-breast cancer activity.

Keywords: 1,2-bis(diphenylphosphino)ethane (PubChem CID: 74267);; 2,6 di-isopropylaniline (PubChem:ID: 32484); 2-(2-Chloroethoxy)ethanol (PubChem CID: 12361); 4-[2-(2-hydroxyethoxy)ethoxy]benzaldehyde (PubChem CID: 11206592); 4-hydroxybenzaldehyde (PubChem CID: 126); Anti-migration; Apoptosis; Cytotoxicity; DNA damage; Dimethyl sulfoxide (PubChem CID: 679); Mitomycin C (PubChem CID: 5746); Necroptosis; Paclitaxel (PubChem CID: 36314); Palladacycles; Palladium (PubChem CID: 23938); acetonitrile (PubChem CID: 6342; bis(acetonitrile)palladium dichloride (PubChem CID: 6093782); dichloromethane (PubChem CID: 61344); sodium acetate (PubChem CID: 517045).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / chemistry
  • Antineoplastic Agents, Phytogenic / pharmacology
  • Antineoplastic Agents, Phytogenic / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Chick Embryo
  • Female
  • Humans
  • MCF-7 Cells
  • Neoplastic Stem Cells / drug effects*
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Paclitaxel / chemistry
  • Paclitaxel / pharmacology
  • Paclitaxel / therapeutic use
  • Palladium / chemistry
  • Palladium / pharmacology
  • Palladium / therapeutic use*
  • Xenograft Model Antitumor Assays / methods

Substances

  • Antineoplastic Agents, Phytogenic
  • Palladium
  • Paclitaxel