Jump to content

Measuring Enzymes at End of Cancer Pathway Predicts Outcome

Recommended Posts

Talks about predicting Tarceva and Taxol outcomes.

ANAHEIM - Researchers at The University of Texas M. D. Anderson Cancer

Center have developed a way to test whether the new targeted therapy Tarceva

and the widely used chemotherapy drug Taxol are effectively killing tumor

cells. They say that with further refinement, the test may make it possible

to accurately assess whether patients are responding to these agents, as

well as potentially others, within days of beginning therapy.

In two different studies being presented at the annual meeting of the

American Association for Cancer Research (AACR), the research team will

describe how the test measures the activity of several members of the

cyclin-dependent kinase (CDK) family of enzymes, which are the triggering

molecules that allow a cell to grow and divide. CDK cell cycle enzymes are

the end target of numerous cellular pathways that are involved in cancer

development and progression, the researchers say.

Before these studies, no one has been able to accurately test the function

of enzymes from a tumor sample, says Naoto Ueno, M.D., Ph.D., an associate

professor in the Breast Cancer Translational Research Laboratory and the

Department of Blood and Marrow Transplantation. "Testing CDK only has been

possible by measuring gene expression, but our industry collaborator has

provided a way that lets us test real enzyme activity within a human tumor

sample," he says. "Our hope is to be able to use this system as a molecular

marker to assess whether an anti-cancer therapy is working."


Sensitivity to Tarceva Depends on CDK2

In the first study, M. D. Anderson researchers found that loss of the CDK2

enzyme strongly correlated with a cancer's sensitivity to Tarceva.

That means testing activity of CDK2, the enzyme that drives cell division,

can reveal whether or not a tumor will respond to Tarceva, says Naoto Ueno,

M.D., Ph.D., an associate professor in the Breast Cancer Translational

Research Laboratory and the Department of Blood and Marrow Transplantation.

If results of this study are verified and validated, "a CDK2 test would

provide the best marker yet for effective use of Tarceva," he says. The only

experimental predictive test currently available is whether lung cancer

cells have a mutation in their epidermal growth factor receptor (EGFR), but

that does not predict response to the targeted therapy in other forms of

cancer, Ueno says.

"We find here that as long as CDK2 is suppressed, the drug works, so

developing an accurate test for CDK2 activity would be a boon for delivering

individualized therapy to patients," he says. Such a test, however, will

require that patients be given the drug for a short period of time so that

the agent's effect on CDK2 activity can be assessed.

In this study, the researchers exposed 10 different human breast cancer cell

lines to varied doses of Tarceva and then measured activity of the CDK

enzymes. They found that tumor cell death was significantly dependent on

whether CDK2 activity was repressed. They then double checked those findings

by "putting CDK2 back," Ueno says. "We found that the effects of Tarceva

were reduced when CDK2 was given back to the cells, so this shows us that

CDK2 is the real target of Tarceva.

"This presents a concept that describes how Tarceva works, and it also shows

that we have a technology that can rapidly measure the true activity of CDK2

in a tumor sample," Ueno says. First author Fumiyuki Yamasaki, M.D., Ph.D.,

a post-doctoral fellow, is presenting the findings at AACR.


Profile CDK to Predict Effectiveness of Taxol

A different research team, headed by Naoto Ueno, M.D., Ph.D., an associate

professor in the Breast Cancer Translational Research Laboratory and the

Department of Blood and Marrow Transplantation, found in a second study

presented at AACR that if activity of several CDK molecules is increased -

not decreased as in the Tarceva finding - then the chemotherapy drug Taxol

appears to effectively kill breast cancer cells.

Taxol, used to treat a wide spectrum of cancers, works by interrupting the

reorganization of the cell that is necessary if it is to divide. While it

was known that the primary effect of the drug is to interfere with assembly

of the spindle that pulls nuclear chromosomes apart during cell division,

Ueno and his colleagues have recently reported that increased activity of

CDK1 correlated with a cell's sensitivity to Taxol.

The CDK enzyme plays a role in cell division, and researchers believe that

it functions in part as a monitor of cell cycle activity. Ueno theorizes

that if something goes wrong during division - such as if Taxol is

interrupting spindle assembly - CDK will become more active in an attempt to

correct the problem.

Working with the Sysmex Corporation of Kobe, Japan, the researchers devised

a test to measure CDK activity and the expression, simultaneously.

They found that monitoring of two isotypes of CDK activity accurately

predicted which tumors would respond to Taxol in the experiments with human

breast cancer cell lines and tumor tissues of human xenograft model.

"This provides solid preclinical evidence that we can use toward development

of a novel device that can measure CDK activity in human tissue within

several hours," Ueno says. He adds that a clinical trial is currently under

way that tests CDK activity both before and after patients with breast

cancer are treated with Taxol.

Link to comment
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Reply to this topic...

×   Pasted as rich text.   Restore formatting

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

  • Create New...

Important Information

By using this site, you agree to our Terms of Use.