Posted on 03/16/2022 9:54:19 AM PDT by Red Badger
Iron Accumulates in Metastatic Tumors
PET imaging (right) shows the accumulation of iron in metastatic tumors growing in the spine and liver of patients with pancreatic ductal adenocarcinoma. Credit: © 2022 Jiang et al.
Originally published in Journal of Experimental Medicine.
https://doi.org/10.1084/jem.20210739
Researchers at the University of California, San Francisco (UCSF), have discovered that cells carrying the most common mutation found in human cancer accumulate large amounts of ferrous iron and that this “ferroaddiction” can be exploited to specifically deliver powerful anticancer drugs without harming normal, healthy cells. The therapeutic strategy, described in a study that was published on March 9, 2022, in the Journal of Experimental Medicine (JEM), could be used to treat a wide variety of cancers driven by mutations in the KRAS gene.
Mutations in KRAS are found in many cancers and are particularly common in pancreatic ductal adenocarcinoma (PDA), colorectal cancer, acute myeloid leukemia, and lung adenocarcinoma. In total, KRAS mutations are thought to cause a quarter of all cancer deaths by activating cell signaling pathways that drive cell proliferation and enhance cell survival. These signaling pathways can be blocked by drugs that inhibit some of the proteins activated by KRAS, but, in addition to killing cancer cells, these drugs are highly toxic to healthy cells and tissues, limiting their use at doses needed to inhibit signaling in cancer cells.
“For example, inhibitors of the MEK1/2 enzymes have shown clinical benefit, but the approach suffers from dose-limiting toxicities in the eye, skin, gut, and other organs,” explains Eric A. Collisson, MD, a professor in the Department of Medicine at UCSF. “Clinical experience has shown that sustainable dosing of these inhibitors is often well below FDA-approved dose, severely hampering the dose intensity achievable in the tumor cell and ultimately limiting clinical efficacy.”
In the new JEM study, first author Honglin Jiang and colleagues develop a method to target MEK inhibitors, and potentially other anticancer agents, to KRAS-driven tumors without harming other, healthy tissues in the body.
The researchers discovered that a wide variety of KRAS-driven tumors show increased activity of genes involved in iron uptake and metabolism, and, in PDA, this increase in gene activity correlated with shorter survival times. PET scans of PDA patients showed that their tumors accumulated high levels of iron. Jiang and colleagues wondered whether this addiction to iron might provide a way to target these cancer cells more precisely.
“We found that the elevated levels of iron, particularly in its ferrous, Fe2+ oxidation state, are driven by oncogenic KRAS, so we hypothesized that mutant KRAS-driven PDA tumor cells might be selectively targeted with a ferrous iron–activatable drug conjugate (FeADC),” explains Adam R. Renslo, a professor in the Department of Pharmaceutical Chemistry at UCSF who led the study.
FeADCs are inactive versions of drugs that break apart in the presence of Fe2+, releasing the drug’s active version. The approach was inspired by anti-malarial drugs like artemisinin that target Fe2+ in the parasite as it invades red blood cells and degrades hemoglobin, producing large amounts of free heme iron.
Renslo and the team synthesized an FeADC version of the FDA-approved MEK inhibitor cobimetinib. Laboratory tests showed that this drug conjugate, named TRX-cobimetinib, had little effect on human skin or retinal cells but was activated inside KRAS mutant cancer cells, inhibiting the KRAS–MEK signaling pathway and blocking cell growth.
The researchers then tested TRX-cobimetinib in several different mouse models of KRAS-driven cancer, including PDA and lung adenocarcinoma. In each case, TRX-cobimetinib inhibited tumor growth just as well as normal cobimetinib. Unlike normal cobimetinib, however, TRX-cobimetinib caused no detectable damage to other, healthy tissues. This lack of toxicity allowed the researchers to combine TRX-cobimetinib treatment with other anticancer drugs. These combination therapies were even better at inhibiting tumor growth with little side effect on other tissues.
“In this study, we describe a therapeutic strategy that enables more tolerable and efficacious combination therapies targeting the signaling pathways in KRAS-driven tumors,” Collisson says. “The discovery of pharmacologically exploitable ferroaddiction in KRAS-driven cancers holds promise to improve the treatment of deadly cancers through a practicable and generalizable approach to FeADC design, development, and clinical testing.”
For more on this research, see Treating Tough Tumors by Exploiting Cancer Cells’ Iron “Addiction.”
Reference: “Ferrous iron–activatable drug conjugate achieves potent MAPK blockade in KRAS-driven tumors” by Honglin Jiang, Ryan K. Muir, Ryan L. Gonciarz, Adam B. Olshen, Iwei Yeh, Byron C. Hann, Ning Zhao, Yung-hua Wang, Spencer C. Behr, James E. Korkola, Michael J. Evans, Eric A. Collisson and Adam R. Renslo, 9 March 2022, Journal of Experimental Medicine. DOI: 10.1084/jem.20210739
Funding: NIH/National Cancer Institute, Congressionally Directed Medical Research Program, Shorenstein, Rhombauer, and Preston Families
Interesting. Microwave resonance, hmm
Perhaps of interest.
The advances in the biological sciences are accelerating thanks to advances in nanotechnology. Once the genetic code of life and the mechanisms of cellular machinery are truly understood and therefor programmable we will a both a bright and horrifying future.
Safe and inexpensive IP6 binds to iron in cancer cells and stops them from dividing https://www.lewrockwell.com/2005/06/bill-sardi/the-overlooked-cancer-cure-from-japan/ . Of course there is no profit to be made by Big Pharma from IP6, so it is ignored by NIH et al.
This is a good article, but the compound, “TRX-cobimetinib,” is not available anywhere to be used today, nor is “TRX” something that can be taken separately, alongside the commonly available “cobimetinib,” unfortunately.
This is a thing for the future that can’t currently be approximated or hacked together in some form for immediate benefit.
Thank you for the alert, though!
Thanks, Bkmk for later.
Starting to look like "iron poor blood" might be a good thing.
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