Trading in the Scalpel for a Sharper Blade

Losing a breast or a lung to cancer leaves a scar, both physical and emotional. But even a biopsy to determine if a tumor is cancerous, or to track a tumor’s response to drugs, brings short-term pain and can miss signs of metastasis. So, the possibility of a scalpel-free biopsy has been something of a holy grail — a way to relieve trauma, speed diagnosis and shrink medical bills.

The ideal non-surgical approach might start with a simple blood draw. Snippets of DNA or RNA detected in the blood could be analyzed for the presence of a tumor; whether it has metastasized and whether it carries mutations for resistance to specific drugs. Such  “liquid biopsies” may now be within reach.   

Kathy Collins, professor of biophysics, biochemistry, and structural biology is launching a startup called KarnaTeq to develop and market a technology to increase the diagnostic power of this new strategy. 

Cancer cells commonly shed bits of DNA into the blood. In several recent cancer clinical trials, researchers isolated DNA from patients’ blood and amplified it for analysis. In a DNA study from one specialized type of treatment, they were able to identify most of the treatment-resistant mutations that had been detected through conventional, invasive biopsies. In fact, DNA sequencing revealed some mutations that the original biopsies had missed, the scientists reported. 

But even a diagnostic tool as promising as this should be more sensitive and informative in order to fulfill the goal of personalized medicine, says Collins. With support from the Bakar Fellows Program, she is developing new techniques to scrutinize the total content of RNA in blood — a strategy that she thinks may add vital clues missed by DNA analysis. 

“RNA is DNA in action,” Collins says. While DNA holds the blueprint for making all the proteins in the body, it hands off to RNA only the instructions that the cell needs. As a result, this “messenger RNA” carries the up-to-date information on cells’ conditions and needs. 

“Sequencing RNA from liquid biopsies will allow us to see not only the state of a cancer but also the molecular signatures of any normal tissue that is in trauma from a treatment,” she says. “Tissue stress is critical to tuning therapy. DNA alone won’t yield this information.” 

In other words, DNA sequences may be easier to find, she says, but they don’t hold all the clues. “We don’t want to bias our understanding by getting only a partial picture.”

To analyze gene sequences retrieved from blood, researchers use a relatively large blood draw. They isolate and amplify the genetic material that has made its way into the blood. With current technology, they can generate millions of individual DNA molecules for analysis, but not all of the RNA.

So far, Collins says, only messenger RNA from intact cells can be analyzed comprehensively. “A profile of other types of RNA such as non-coding RNA and RNA from pathogens would give an unbiased, ‘wide-field’ snapshot of current health status.”

Collins has developed a new technology that employs a type of enzyme that she has studied for more than 20 years. It is called a reverse transcriptase because it can translate, or transcribe, RNA into DNA — the reverse of the classic “Watson and Crick” DNA to RNA process.

HIV and other retroviruses use their own reverse transcriptase to transcribe their RNA into DNA and then integrate it into a host’s DNA strands. The invaded cell then becomes an agent of its own destruction, blindly replicating the virus’s genetic instructions along with its own, enabling the virus to multiply and spread. 

Through modifications of an ancient reverse transcriptase, Collins can retrieve a comprehensive inventory of RNA. Because of the unique way the enzyme engages RNA molecules, it can access folded strands generally invisible to other techniques. The transcribing process captures more of the RNA than other methods and is less error-prone. 

She is particularly interested in applying the new strategy to study RNA held in bubble-like vesicles, called exosomes, secreted by cancer cells into the blood. Very little is known about them, but many scientists suspect that DNA, RNA and other molecules packed inside the vesicles can provide unique insights into cancer’s progress in a patient.

With guidance from Bakar Fellows mentors, Collins aims to advance research on exosomes and other potential troves of genetic information, and expects her new RNA analysis technology will be useful in a range of basic research and clinical applications. 


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The Bakar Fellows Program at UC Berkeley fosters faculty entrepreneurship in the STEM+ fields including Engineering, Computer Science, Chemistry, Biological Sciences, Physical Sciences, and Architecture.  Bakar Fellows receive discretionary research support to mature and translate their ground-breaking discoveries and innovations into commercial solutions. 
For more information, see http://bakarfellows.berkeley.edu.