The reason behind the radiation treatment resistant.

Approximately 50% of all cancer patients will receive radiation therapy (RT) during the course of their illness. In most solid tumors, hypoxia occurs to some degree as a result of several factors, including the rapid growth rate of cancer cells and the highly disorganized/inefficient vasculature.

X-rays and electron beams are the main forms of radiation to treat cancer. Most of the damage is not caused by the radiation energy directly damaging tumor cells (Direct effect), but rather by the radiation energy creating highly reactive substances, especially so-called free radicals, that damage important structures in cells leading to cell death (Indirect effect).

Fig.1: Direct and Indirect Effects of Radiation

The amount of oxygen inside a cell influences its susceptibility to radiation damage. Hypoxia (low oxygen levels) make cells more resistant.


How our solution will overcome the issue.

New radiosensitizer, KRC-01, overcomes this problem. KRC-01 contains 3% hydrogen peroxide (H2O2) and 1% sodium hyaluronate. H2O2 is the active ingredient for this radiosensitizer and is the only agent known to be capable of inactivating antioxidative enzymes and producing an excess amount of H2O2 to induce lysosomal membrane instability leading to apoptosis (H2O2 effect). Sodium hyaluronate delays decomposition of H2O2 and maintains a high partial pressure of oxygen in the tumor up to at least 24 hours following an intratumoral injection of the KRC-01 as well as exerts the effect of mild pain killer at the injection site.

Fig.2: Treatment Rationale of KRC-01

When KRC-01 is injected into a tumor, antioxidative enzymes, such as peroxidases and catalases, that are especially abundant in the radioresistant tumor begin to break H2O2 down into water and oxygen accompanying an inactivation of these antioxidative enzymes. Then, the energy from the sudden radiation dose splits some of the remaining H2O2 into highly reactive hydroxyl radicals (•OH) which bind to and damage important parts of the tumor cells.

The newly released oxygen enhances this damage. One mechanism is by causing sections of DNA to which •OH radicals are bound to suffer double-strand breaks. This usually makes the DNA unrepairable and results in cell death.

Also, high levels of H2O2 neutralize the antioxidative enzymes, such as peroxidases and catalases, that protect tumor cells from the oxidative damage H2O2 can cause.

Fig.3: Mode of Action of KRC-01