By Angela Grant
CMB guest writer

The frustrations of setting up a new lab were quite obvious 10 minutes into our interview when the lab manager rushed into the office and whispered in a panicked voice, “The tubing to the nitrogen tank blew a hole in it and the room is filled with nitrogen.” Dr. Carla Van Den Berg, Assistant Professor in the Division of Pharmacology/Toxicology program, sighed. “Hopefully, our brand new microscope is okay since the nitrogen gas was supposed to be suspending the table it sets on,” was all she said.  This is simply one small bump in the road in the past year.

When the lab is finally in order, Van Den Berg’s research generally spans two areas of breast cancer research – one being, to study the effects of Insulin-like Growth Factor-I  (IGF – I) on breast cancer cells.  IGF-I is similar in structure to insulin.  Normally, it plays an important role in prenatal growth and development and a lesser role in glucose metabolism.  It can also be important to tumor cells.  Many types of cancers, including breast, prostate and colon cancers, use IGF-I to promote their growth and survival.  Dr. Van Den Berg initially became interested in how it protects cancer cells from chemotherapy treatment when other clinicians proposed to administer IGF-I to cancer patients to regenerate nerve cells.  Some patients experience numbness in their extremities after receiving certain chemotherapy drugs and this occurs because of the unwanted toxicities of chemotherapy. Dr. Van Den Berg and her mentor were concerned that although it may improve neuropathic symptoms in cancer patients it could also have detrimental effects on the tumors’ response to treatment.

The second area of interest in the lab is an intracellular kinase that is activated by chemotherapy drugs and in turn assists in killing cells.  This protein is called JNK (c-Jun N-terminal kinase).  JNK is also be activated by other stresses such as heat, osmotic stress or cytokine exposure. “Our observation is that IGF activates JNK in breast cancer cells.  Other researchers have reported that JNK can signal cells to move.  Interestingly, this type of movement is important for tumor cells to become metastatic (i.e. move from the place they started to other sites in the body).  Metastasis is the most challenging part of breast cancer treatment.  We are using mouse models to understand the importance of JNK in both tumor development and metastasis,” she said.  Hence, both IGF-I and JNK are somewhat double-edged swords but…. “Welcome to cancer,” said Van Den Berg.

Her interest in cancer research began during her oncology residency training at the Audie Murphy VA Hospital and the UT Health Sciences Center in San Antonio. “I decided that I didn’t understand what our treatments were doing to our patients, and so I wanted to study this in more detail.” One of her fellowships was with an oncologist/basic scientist who studied IGF-I in breast cancer. “My goal is to figure out why chemo drugs sometimes don’t work and also to identify better and less toxic treatment alternatives,” she said. After her fellowship training, Dr. Van Den Berg was an Assistant/Associate Professor at the University of Colorado Health Sciences Center in the School of Pharmacy.  There she received research funding from organizations like the Susan G. Komen Foundation, the Department of Defense, the National Institute of Health, and others.  Just before her move to Austin, she received a grant from The National Institute of Health, which gave her research on JNK a highly enthusiastic score. Van Den Berg’s current lab consists of one postdoctoral fellow, four graduate students, two research assistants and a summer undergraduate student.  All but two of these people started in the lab just this summer.  Once the growing pains have started to subside, Dr. Van Den Berg said that she looks forward to taking advantage of the many excellent resources here and interacting with various faculty at UT, Austin.

Dr. Carla Van Den Berg
h5>Dr. Carla Van Den Berg