Microtubules identified as promising new cancer fighter
To make new cells, we have to divide existing ones. This is a continuous, frequent and ubiquitous process which starts at conception.
[Dec. 7, 2022: Omar Jamshed, Center for Genomic Regulation]
To make new cells, we have to divide existing ones. This is a continuous, frequent and ubiquitous process which starts at conception and ends at death. (CREDIT: Creative Commons)
To make new cells, we have to divide existing ones. This is a continuous, frequent and ubiquitous process which starts at conception and ends at death. There are an estimated 37 trillion cells in the tissues and organs of the human body, each of which originates from one cell dividing into two.
When cell division goes wrong, it can lead to the creation of new cells with an abnormal number of chromosomes, a phenomenon known as aneuploidy. The frequency at which chromosome segregation errors occur is known as chromosomal instability (CIN). In some cases, for example a developing embryo, this can promote spontaneous abortion and in others, it can contribute to human diseases such as cancer. Aneuploidy and CIN are hallmarks of particularly aggressive tumours.
Researchers study cell division to understand how chromosome segregation occurs without mistakes every time a cell divides. They also investigate why and how mistakes can occur and generate aneuploid cells.
Faithful chromosome segregation is fully dependent on the correct attachment of the chromosomes to the mitotic spindle, the molecular machinery that pulls chromosomes to opposite sides of a cell. The spindle is formed of microtubules, long-hollow tubes made from proteins. Microtubules must remain stable enough to move and align the chromosomes, but also dynamic enough to allow for correction of the erroneous attachments before chromosomes are pulled apart and segregated.
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The dynamics of microtubules and how they are finely regulated are fundamental to understanding how cells divide. Their importance is underscored by the identification of a compound in the early 1970s that is still currently used in chemotherapy and directly stabilizes microtubules, causing cancer cells to self-destruct.
For ICREA Research Professor Isabelle Vernos, Group Leader in the Quantitative Cell Biology research programme at the Centre for Genomic Regulation (CRG), how microtubule dynamics is regulated during cell division in cancer is still not fully understood and could reveal new mechanisms to exploit. Her latest study, published last week in Nature Communications, reveals potential new viable therapeutic targets in cancer.
Microtubules undergo various modifications in different cell types and tissues that finely define their specific functions. In this work, the researchers identified tubulin tyrosine ligase like 11, also known as TTLL11, an enzyme that specifically modifies the spindle microtubules by adding glutamate chains to the surface of the microtubule. This is a process known as polyglutamylation,
Mitotic spindles with microtubules (red) attached to chromosomes (blue) during cell division. Cells with normal TTLL11 function (right) have normal rates of microtubule polyglutamylation (green) while cells without TTLL11 (left) are unmodified. (CREDIT: Isabelle Vernos/CRG)
They found that microtubule polyglutamylation defines the dynamism and stability of the spindle microtubules, which in turn secure the faithful segregation of the chromosomes. Time-lapse imaging revealed that without TTLL11, cells and zebrafish embryos were much more likely to undergo chromosome segregation errors.
When the researchers examined TTLL11 levels in cancer compared to healthy tissue using data from the Cancer Genome Atlas, a public database that includes molecular characteristics of more than 20,000 primary cancer matched with normal samples spanning 33 cancer types, they found that TTLL11 was significantly downregulated in every single one of these tumours compared to the corresponding normal tissue.
TTLL11 localizes to the spindle and drives MT polyglutamylation in mitosis. Immunofluorescence images of metaphase spindles in control and siTTLL11 HeLa cells, showing PolyE (green), tubulin (red) and DNA (blue). Scale bars, 10 μm. (CREDIT: Nature Communications)
“We found that low levels of TTLL11 are highly specific to cancer. This is exciting because it reveals another layer to how microtubules are regulated during cell division in cancer. Drugs that interfere with microtubule dynamics are already one of the most successful first-line cancer therapies. If this turns out to be a viable therapeutic target, our findings pave the way to the creation of a new generation of drugs that are more precise and effective than conventional treatments,” says Dr. Vernos.
The authors of the study also explained why low levels of TTLL11 affect cell division.
zfTTLL11 is required for early embryonic zebrafish development. Immunofluorescence image of a zebrafish embryo (at 4 h post fertilization [hpf]), showing PolyE (green), tubulin (red). Scale bar, 20 μm. Representative image of N = 3 independent experiments. (CREDIT: Nature Communications)
“Microtubules need to establish stable connections with the chromosomes to align them and pull them apart, but these connections also need to be flexible enough to be corrected on time to avoid any errors during segregation. Microtubules in cancer cells have low levels of TTLL11, making them too stable thereby favouring the segregation of chromosomes in the presence of attachment errors that will result in aneuploid cells. It remains to be demonstrated whether this is a mechanism being exploited by cancer cells to grow and generate diversity through random chromosome segregation errors. This constitutes new exciting avenues of research,” explains Dr. Vernos.
The research is published in Nature Communications and is led by Dr. Isabelle Vernos at the CRG. Collaborators include ICREA Research Professors Dr. Verena Ruprecht and Dr. Luis Serrano, also at the CRG, as well as Carsten Janke at Institut Curie. Other authors include Ivan Zadra, Senda Jimenez, Miquel Anglada, Carolina Segura and Zachary Compton.
Note: Materials provided above by Center for Genomic Regulation. Content may be edited for style and length.
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