We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Advertisement
Copper Cysteamine Inhibits the Proliferation of Deep-Seated Tumors
News

Copper Cysteamine Inhibits the Proliferation of Deep-Seated Tumors

Copper Cysteamine Inhibits the Proliferation of Deep-Seated Tumors
News

Copper Cysteamine Inhibits the Proliferation of Deep-Seated Tumors

Read time:
 

Want a FREE PDF version of This News Story?

Complete the form below and we will email you a PDF version of "Copper Cysteamine Inhibits the Proliferation of Deep-Seated Tumors"

First Name*
Last Name*
Email Address*
Country*
Company Type*
Job Function*
Would you like to receive further email communication from Technology Networks?

Technology Networks Ltd. needs the contact information you provide to us to contact you about our products and services. You may unsubscribe from these communications at any time. For information on how to unsubscribe, as well as our privacy practices and commitment to protecting your privacy, check out our Privacy Policy

Wei Chen, professor of physics at The University of Texas at Arlington, is the senior author of two papers detailing the effects of copper cysteamine, a next-generation cancer photodrug invented in Chen’s laboratory.

The first article, “A new type of cuprous-cysteamine sensitizers: Synthesis, optical properties and potential applications,” was published in Materials Today Physics. It reports that copper cysteamine photosensitizers, or light-activated molecules, exhibit a range of luminescent properties, allowing them to produce more reactive oxygen species that kill cancer cells.

The second, “Study of copper-cysteamine based X-ray induced photodynamic therapy and its effects on cancer cell proliferation and migration in a clinical mimic setting,” was published in the journal Bioactive Materials. The study reports that copper cysteamine inhibits the proliferation of deep-seated tumor cells and minimizes toxic side effects associated with cancer treatment that impact healthy cells.

Nil Kanatha Pandey, a Ph.D. student in Chen’s lab, is among the coauthors of both papers.

Treating hard-to-reach tumors


With the development of nanotechnology, photodynamic therapy (PDT) has become a promising alternative to traditional cancer treatments. PDT combines photosensitive molecules, or photosensitizers, with light at the site of a tumor to produce a powerful oxygen species that destroys cancer cells.

However, light-induced PDT, including ultraviolet, visible and near-infrared light bands, has poor penetration in human tissue. The deeper that a tumor is buried in tissue, the less effective PDT becomes.

Chen’s next-generation photosensitizer produces reactive oxygen species from stimulation not only by general light, but also by ultrasound, X-rays and microwaves. The drug’s responsiveness to various stimulants allows it to be used to treat superficial cancers as well as those located deep within tissue.

Reduced toxicity for cancer patients


A common goal among cancer drug developers is to reduce damaging side effects caused by treatment. Chen’s photosensitizer could reduce two major risks: radiation and exposure to sunlight.

Radiotherapy is one of the most common cancer medications, but radiation can cause damage to healthy cells located near the site of treatment. Because copper cysteamine is activated by X-rays, Chen’s team combined the photosensitizer with radiotherapy techniques to reduce radioactive doses and side effects. The results were promising.

“The copper cysteamine ensured the effectiveness of the radiotherapy treatment at lower doses of radiation,” Chen said. “Our research demonstrates that copper cysteamine could be applied to radiotherapy in a clinical setting and result in a safer treatment for patients.”

Most photosensitizers are very toxic under sunlight, requiring patients to be protected from light for some time after treatment. Chen’s research revealed that the copper cysteamine photosensitizer does not produce toxic reactive oxygen species under sunlight and could reduce patients’ risk of light exposure post-treatment.

“Our goal is to develop a method of PDT that is potent and safe,” Chen said. “This new material will open the door to more effective treatment for a range of cancer diagnoses.”

References

Chen X, Liu J, Li Y, et al. Study of copper-cysteamine based X-ray induced photodynamic therapy and its effects on cancer cell proliferation and migration in a clinical mimic setting. Bioactive Materials. 2022;7:504-514. doi: 10.1016/j.bioactmat.2021.05.016

Wang Y, Alkhaldi ND, Pandey NK, et al. A new type of cuprous-cysteamine sensitizers: Synthesis, optical properties and potential applications. Materials Today Physics. 2021;19:100435. doi:10.1016/j.mtphys.2021.100435


This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

Advertisement