New study finds link between difficulty identifying emotions and higher chronic pain levels
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Updates every hour. Last Updated: 27-Oct-2026 00:16 ET (27-Oct-2026 04:16 GMT/UTC)
A research team has identified a promising new therapeutic strategy for idiopathic pulmonary fibrosis (IPF), showing that blocking two proteins can halt and even reverse lung scarring in pre-clinical models. IPF is a progressive disease in which scar tissue builds up in the lungs, making it increasingly difficult to breathe. The disease affects an estimated 100,000 people in the United States, with about 30,000 to 40,000 new cases diagnosed each year, according to the National Institutes of Health.
Researchers at the University of British Columbia and BC Cancer have developed a new way to target proteins long considered “undruggable,” opening the door to new treatments for prostate cancer and other serious diseases. Known as intrinsically disordered proteins, these molecular shapeshifters are extremely difficult to target with medication due to their flexible and ever-changing structure. They play a central role in a wide range of diseases—including cancer, neurodegenerative disorders, heart disease and autoimmune conditions—yet only a handful of medications currently exist that can target them. In a study published today in Nature Signal Transduction and Targeted Therapy, the researchers demonstrate a new approach for designing drugs that bind more strongly to these proteins and block their disease-causing activity. In some cases, the compounds they developed bound up to a million times more tightly than any previously reported.