A recent study performed
by Stefanie Jeffrey, MD (professor of surgery and chief of
surgical oncology research at the Stanford University School of Medicine) and
her research team has brought new insight into the heterogeneity of cancer
cells and how we may be able to treat them. Through the use of two relatively
new technologies (the Magsweeper and the PCR microfluidic chip) the researchers
were able to isolate and sequence 95 genes from the circulating tumor cells of
50 patients with breast cancer. Circulating tumor cells, or CTCs, are a rare
type of red blood cell believed to help disseminate cancer from organ to organ
throughout the body. The results of the study reflected a surprising amount of
genetic diversity in CTCs. “In the patients, we ended up with a subset of 31
genes that were most dominantly expressed,” said Jeffrey. “And by looking at
levels of those genes, we could see at least two distinct groups of circulating
tumors cells.” The researchers were able to divide the CTCs into as many as
five groups, depending on which genes were used, each with different
combinations of genes turned on and off. The diversity among these CTCs
suggests that a single biopsy of a patient’s tumor does not necessarily indicate
all of the molecular changes driving the cancer forward and helping it to spread.
As we continue in our efforts to learn more about cancer and how to treat it,
we must keep in mind that different cells may require different therapies.
According to an article published on the Stanford
University School of Medicine website, this study is “the first time that
scientists have used high-throughput gene analysis to study individual CTCs,
and opens the door for future experiments that delve even more into the cell
diversity. The Stanford team is now working on different methods of using CTCs
for drug testing as well as studying the relationship between CTC genetic
profiles and cancer treatment outcomes. They’ve also expanded their work to
include primary lung and pancreatic cancers as well as breast tumors.”
Sources
1. Eurekaalert.com: “Not all tumor
cells are equal: Stanford study reveals huge genetic diversity in cells shed by
tumors” < http://www.eurekalert.org/pub_releases/2012-05/sumc-nat050312.php>
2. Med.stanford.edu: “Not all tumor cells are equal:
Study reveals genetic diversity in cells shed by tumors” < http://med.stanford.edu/ism/2012/may/jeffrey.html>
3. Plosone.org: “Single Cell Profiling of
Circulating Tumor Cells: Transcriptional Heterogeneity and Diversity from
Breast Cancer Cell Lines” < http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0033788>
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