{"id":6974,"date":"2021-10-06T14:13:38","date_gmt":"2021-10-06T19:13:38","guid":{"rendered":"https:\/\/www.wisconsin.edu\/all-in-wisconsin-new\/?post_type=campus_story&p=6974"},"modified":"2021-10-06T14:13:38","modified_gmt":"2021-10-06T19:13:38","slug":"uw-madison-breast-cancer-researchers-learn-how-to-teach-an-old-drug-new-tricks-to-help-patients","status":"publish","type":"campus_story","link":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/story\/uw-madison-breast-cancer-researchers-learn-how-to-teach-an-old-drug-new-tricks-to-help-patients\/","title":{"rendered":"UW-Madison breast cancer researchers learn how to teach an old drug new tricks to help patients"},"content":{"rendered":"
\"Photo
Beth Weaver wanted to know if there was a way to predict who would benefit from Taxol and who might not, to spare these patients the side effects of the potent chemotherapy drug. COURTESY OF UW CARBONE CANCER CENTER<\/figcaption><\/figure>\n

Paclitaxel, or Taxol, is an old standby drug in the oncologist\u2019s tool belt. Yet only about half of breast cancer patients treated with the drug see their tumors shrink or disappear, and doctors and researchers have no way of knowing which patients will benefit.<\/p>\n

But that may soon change.<\/p>\n

Published Sept. 8 in Science Translational Medicine<\/a>, an analysis of patient samples by a team of researchers led by University of Wisconsin\u2013Madison Professor of Cell and Regenerative Biology Beth Weaver has uncovered a key feature of breast cancers that renders them either vulnerable or resistant to paclitaxel treatment. And it could be used to help identify which patients are most likely to see success.<\/p>\n

\u201cIt\u2019s a huge problem,\u201d says\u00a0Weaver<\/a>, a member of the UW Carbone Cancer Center. \u201cNearly half of patients who get this drug can be subjected to some pretty substantial side effects without any therapeutic benefit.\u201d<\/p>\n

Key to the finding is something called chromosomal instability, found in about half of breast cancers and caused by errors that take place when cells improperly divide.<\/p>\n

Almost all cells in the body divide. This is how organisms grow and adapt. During that process, called mitosis, the original cell\u2019s genetic material \u2014 in the form of chromosomes \u2013 is equally distributed or \u201csegregated\u201d between two identical daughter cells. When it doesn\u2019t go smoothly, chromosome distribution becomes unbalanced or \u201cmis-segregated,\u201d and each daughter cell contains an incorrect amount of genetic material. This is a hallmark of cancer.<\/p>\n

Low rates of mis-segregation, called chromosomal instability, can encourage cells to begin to divide unchecked and cause tumors. However, if this mis-segregation is extreme it causes the cells to die.<\/p>\n

The researchers found that patients with cancers exhibiting high levels of chromosomal instability were more sensitive to paclitaxel and had better tumor suppression, meaning it could be the elusive predictor of paclitaxel success.<\/p>\n

\u201cThat would be huge,\u201d Weaver says. \u201cYou could measure for chromosomal instability on leftover tissue from a diagnostic biopsy, which patients need to have anyway, and potentially use that tissue for a biomarker test.\u201d<\/p>\n

Weaver, an expert in cell division and chromosome segregation, has studied paclitaxel in the lab ever since her graduate school days, but has gradually shifted her focus to examine how the commonly used chemotherapy works in the cells of breast cancer patients.<\/p>\n

Researchers once believed that paclitaxel worked by preventing cancer cells from dividing. But in a previous study of patients on a standard, high-dose paclitaxel regimen, Weaver, her\u00a0Carbone colleague Mark Burkard<\/a>, and their research teams\u00a0found that model didn\u2019t hold up<\/a>. Instead, they found that the drug amplified mis-segregation in dividing cancer cells.<\/p>\n

\u201cThat suggested to us that the way we thought Taxol worked for the last 30 years was wrong, and that was a big question mark and concern,\u201d Weaver says. It led her and her team to the hypothesis that paclitaxel may exert its anti-cancer effects by causing or taking advantage of chromosome instability.<\/p>\n

In the latest study, the research team was able to study difficult-to-obtain breast cancer samples that captured a very specific moment in time in the life cycle of cells from breast cancer patients being treated with a typical low-dose paclitaxel regimen. Then they looked at what was happening during cell division.<\/p>\n

During normal cell division, the cell forms structures called spindles, which attach to chromosomes at the center of the cell and then, like little ropes, pull the genetic material apart as the cell begins to split into two. This helps ensure the right number of chromosomes stay with the original cell and get added into the new daughter.<\/p>\n

These spindles are anchored to a single location at either end of the cell, or at two poles. However, in the samples from patients treated with paclitaxel, the spindles formed multiple poles in the cells. These cells faced one of two fates: The abnormal spindles were maintained throughout cell division, or the spindles were eventually \u201cfocused\u201d back down into traditional bipolar spindles.<\/p>\n

When the abnormal multiple spindles were maintained, the cells died and tumors regressed. When the spindles were focused back into bipolar spindles, the cells generally became more resistant to paclitaxel.<\/p>\n

\u201cUnderstanding that this focusing is a major mechanism of resistance opens the door to first identifying novel drug targets and then developing drugs that will sensitize to paclitaxel,\u201d Weaver explains.<\/p>\n

Taken as a whole, the findings may represent a major step forward in the cancer community\u2019s understanding of paclitaxel. And even though many non-chemotherapy therapeutics, such as targeted therapies and immunotherapies, are in development to treat breast cancer, Weaver says there\u2019s a huge benefit to trying to teach this old drug some new tricks.<\/p>\n

\u201cWhat we\u2019re really trying to do is turn this conventional chemotherapy into personalized medicine,\u201d Weaver said. \u201cThat would be the best of all worlds because paclitaxel is widely used, it\u2019s inexpensive, and clinicians have a ton of experience with it. If we could just target it to the right patients, it would be a huge improvement in cancer care.\u201d<\/p>\n","protected":false},"excerpt":{"rendered":"

Paclitaxel, or Taxol, is an old standby drug in the oncologist\u2019s tool belt. Yet only about half of breast cancer patients treated with the drug see their tumors shrink or disappear, and doctors and researchers have no way of knowing which patients will benefit. But that may soon change. Published Sept. 8 in Science Translational […]<\/p>\n","protected":false},"author":15,"featured_media":6975,"comment_status":"closed","ping_status":"closed","template":"","institution":[103],"story_category":[],"class_list":["post-6974","campus_story","type-campus_story","status-publish","has-post-thumbnail","hentry","institution-uw-madison"],"_links":{"self":[{"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/campus_story\/6974","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/campus_story"}],"about":[{"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/types\/campus_story"}],"author":[{"embeddable":true,"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/users\/15"}],"replies":[{"embeddable":true,"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/comments?post=6974"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/media\/6975"}],"wp:attachment":[{"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/media?parent=6974"}],"wp:term":[{"taxonomy":"institution","embeddable":true,"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/institution?post=6974"},{"taxonomy":"story_category","embeddable":true,"href":"https:\/\/www.wisconsin.edu\/all-in-wisconsin\/wp-json\/wp\/v2\/story_category?post=6974"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}