Researcher Spotlight: Adrian Salic, Ph.D.

Adrian Salic, PhD in the labPublished February 4, 2020

Adrian Salic, Ph.D. | Harvard Medical School

PKD Foundation (PKDF): How did you first get involved in PKD research?

Adrian: My lab has had a longstanding interest in studying signaling processes that take place in the primary cilium, a structure that plays the role of a cellular antenna, receiving and interpreting numerous different stimuli. While studying primary cilia, I became aware of their crucial role in PKD, and I realized there is much to learn about how cilia defects lead to PKD.

PKDF: What are you working on currently?

Adrian: We are trying to understand the mechanisms of signal transduction in primary cilia, as they relate to cystogenesis, and to less frequent birth defects. We are also developing novel chemical tools to visualize various cellular components (DNA, RNA, proteins, lipids).

PKDF: What would you like the patient community to know about your research?

Adrian: To find a cure for any disease, we need an understanding of the molecular mechanisms behind it: how a process functions normally, and how it leads to disease when the process is impaired, for example by genetic mutation. Basic scientists like myself are trying to decipher these mechanisms and help devise new therapies based on this molecular understanding.

PKDF: What excites you most about this research?

Adrian: In the past, I have worked on biological problems with a less direct disease connection. This is the first time that our work is relevant to an important health problem. This gives me a great feeling of satisfaction that we can hopefully contribute to speeding up the discovery of a cure for PKD.

PKDF: What are some of your personal interests outside of research?

Adrian: I enjoy spending time with family and friends, reading, traveling, visiting art museums, and listening to live music.


Check out Dr. Salic’s grant and others funded by PKDF here!

PKD Foundation is the largest private funder of PKD research in the U.S. Since 1982, we’ve invested close to $50 million in more than 1,300 research, clinical and scientific grants, fellowships and scientific meetings. Each year, The Foundation identifies and supports the work of scientists and researchers from around the world who look for ways to treat and eventually cure PKD.

Our vision is to end PKD. Donations help fund necessary research that leads to more effective treatments and ultimately a cure for PKD.


  1. Nicole

    Thank you so much for your work! I have 3 children and 9 grandchildren that may inherit my PKD…

    I work with our local chapter fundraising for the PKD Foundation and am so happy to see the research we are funding!

  2. Amy E.

    Thank you for your hard work so that I and my family will have longer healthier lives!

  3. Rosemarie Bartus

    Thank you so much for your work and am very hopeful that my children and grandchildren will not have to suffer from this disease as my husband did.


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