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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  TLTFF

Theralase Technologies Inc. is a Canada-based clinical-stage pharmaceutical company. The Company is engaged in the research and development of light activated compounds and their associated drug formulations. The Company operates through two divisions: Anti-Cancer Therapy (ACT) and Cool Laser Therapy (CLT). The Anti-Cancer Therapy division develops patented, and patent pending drugs, called Photo Dynamic Compounds (PDCs) and activates them with patent pending laser technology to destroy specifically targeted cancers, bacteria and viruses. The CLT division is responsible for the Company’s medical laser business. The Cool Laser Therapy division designs, develops, manufactures and markets super-pulsed laser technology indicated for the healing of chronic knee pain. The technology has been used off-label for healing numerous nerve, muscle and joint conditions. The Company develops products both internally and using the assistance of specialist external resources.


TSXV:TLT - Post by User

Comment by CancerSlayeron Mar 16, 2023 3:46pm
214 Views
Post# 35343375

RE:RE:RE:RE:RE:About the addition of up to 9 CSS ...

RE:RE:RE:RE:RE:About the addition of up to 9 CSS ...

Eoganacht wrote: Hi CancerSlayer - Thanks for that. It's a new area for me. I'm not sure if this ROS resistance applies to pdt or not because of the violence of the reaction when the PS is exposed to light and the immediacy of damage to surrounding tissue.

"PDT uses a PS molecule as a prodrug that under light irradiation generates an intense blast of reactive oxygen species (ROS) such as superoxides (O2−), hydroxyl radicals (HO−), and/or singlet oxygen 1O2, which eventually cause cytotoxic damage to biomolecules adjacent to the PS."

"TLD1433 is known to generate reactive oxygen species (ROS) with high quantum efficacy in many cancer cell lines."

TLD1433 Photosensitizer Inhibits Conjunctival Melanoma Cells in Zebrafish Ectopic and Orthotopic Tumour Models



 

I agree...the intensity & immediacy of ROS production using our type of ACT overwhelms a cancer cell.  Imo, the ability of a cancer cell to survive our ACT more likely relates to inadequate delivery of PS to the cancer cell (causing a sub-cytotoxic level of PS within the cell) & not the mechanism of action of our PS/PDT.  The key for success in this case would be maximizing the delivery of PS into every cancer cell.  

The research to date seems to point to the fact that ROS production plays a key role in cancer cell death for various therapies (I.e. chemo & radiotherapy), & the data to date seems to demonstrate that our ACT does it very effectively & efficiently w/o the heavy collateral damage.  

I see lots of opportunity for Pharma/other therapies wanting to ride on our coattails, exploring/using our ACT as both a stand-alone & as an adjuvant/combo option.  Regarding the latter, one could not only take advantage of having additional/instantaneous ROS production, but also have the potential advantage of destroying cancer synergistically....or at least having the ability of utilizing multiple cancer-destroying pathways (direct & immunologic) for their additive gains.  Until a stand-alone can independently beat cancer, the combo approach is going to be the go-to option for many cancers in the foreseeable future imo.  Our ACT should make an excellent partner. 

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