SCIENCE & TECHNOLOGY

ACS MEETING NEWS TARGETING TELOMERASE Researchers believe enzyme could be a nearly universal target for anticancer drugs STU BORMAN, C&EN WASHINGTON

TELOMERASE MAY BE A NEARLY

universal anticancer drug target: Inhibitors of this human enzyme might be able to treat most cancers without significant

side effects. That theory hasn't been verified

yet clinically, but it was nevertheless the overarching theme of a Division of Medicinal Chemistry session on telomerase at last month's American Chemical Society national meeting in San Francisco. The session was or­ganized by assistant professor of me­dicinal chemistry Brian S.J. Blagg of the University of Kansas, Lawrence, and assistant professor of medicinal chemistry and natural products Mi­chael B. Jarstfer of the University of North Carolina School of Pharmacy, Chapel Hill. Speakers described their efforts to design inhibitors of telomerase and to bet­ter understand the structure and function of the enzyme and its target.

Telomerase is an enzyme that cata­lyzes the lengthening of telomeres, DNA structures found at the ends of chro­mosomes. Telomeres are mostly double-stranded DNAs with a repeating TTAGGG se­quence on one strand and a complementary sequence on the matching strand. With all that re-petitiveness, you might expect them to be boring. But they're really not, because this repetitive part of the chromosome just might hold the key to treating cancer more effectively.

The potential role of telomeres as near-universal anticancer targets stems from their tendency to shrink over time. When cells di­vide by mitosis, their chromosomes are rep-

licated, and telomeres get shorter with each replication. This shortening occurs because the DNA polymerases that catalyze replica-

IN THE CLINIC Line structure and molecular model of Geron's lipid-conjugated N3' · P5' thiophosphoramidate human telomerase inhibitor GRN163L C is gray; H, off-white; N, blue; P, brown; and S, yellow. Β is a nucleic acid base.

tion can't copy the very end of each telomere, making new telomeres 50 to 100 base pairs shorter each time chromosomes are copied. W h e n telomeres get critically short, cells stop dividing and commit suicide.

DUPLEX BOUND Compounds like this are being elaborated

into libraries by Friedman's team in an effort to identify small molecules that bind to the RNA-DNA duplex that

forms during telomere extension.

Cancer cells divide more than normal somatic cells. If their telomeres were to shorten with each mitotic event and not be restored, they might have to commit suicide, too, which would crimp their propensity to proliferate and take over tissues.

So most cancer cells have developed a vampirelike means of maintaining their telomeres. To live forever, so to speak, they express telomerase, an enzyme that cata­lyzes replacement of the telomeric region lost during replication.

Telomerase has both an R N A subunit, which serves as a template for telomere lengthening, and a catalytic protein sub-unit, which catalyzes the extension reaction. Telomerase is expressed only in cells that proliferate a lot, such as embryonic cells, germline cells, and some stem cells, in addi­tion to cancer cells. It's not usually expressed in nonproliferative normal somatic cells.

This is a potentially useful distinction. "Since telomere maintenance is one of the

absolute requirements for a cancer cell to continue dividing, it makes sense that if you knock out telomere maintenance—which most cells don't have to worry about be­cause they're not dividing frequently—then cancer cells won't be able to proliferate," Jarstfer said. So if you use a drug to inhibit telomerase, you'll probably attack the cancer and perhaps see side effects in some other proliferative cells, but you're not likely to see adverse effects in most body cells because they don't express telomerase. Voilà: selec­tive anticancer activity.

TELOMERASE CAN be targeted in vivo via various means, such as small organic mol­ecules, oligonucleotide-based compounds, or immunotherapeutic agents. Speakers at the meeting session discussed some of these approaches.

For example, associate professor of phar­maceutical sciences Simon H. Friedman and

If you use a drug to inhibit telomerase, you're not likely to see adverse effects in most body cells because they don't express the enzyme. 3 2 C & E N / OCTOBER 9. 2006 W W W . C E N - 0 N L I N E . O R G

coworkers at the University of Missouri, Kansas City, are trying to inhibit telomerase by using small molecules to target the RNA-DNA duplex that forms between telomer-ase's R N A template strand and the telomere's terminal DNA strand at the start of the telomere extension process.

Friedman and coworkers believe that small molecules might inhibit telomerase ei­ther by distorting the duplex, which would make addition of new bases difficult, or by overstabilizing the duplex, which would hinder unwinding, an essential step in the D N A replication pro­cess. They also hope the studies will help them identify key interactions between the small molecules and surrounding telomer­ase surfaces.

H e and his coworkers are current ly making large libraries of small molecules that can be screened for inhibitory activity "We're aiming for a low- or subnanomolar inhibitor, and we haven't gotten there yet," Friedman said.

Jarstfer and coworkers also want to in­hibit telomerase, but they're trying to do so with oligonucleotides instead of with small organic molecules. Their strategy is to use oligonucleotides to block specific RNA-protein contacts that are required for the protein and R N A components of telomerase to assemble properly in cells. Oligonucleotides interfere with correct as­sembly of the telomerase complex, making the complex incapable of catalyzing telomere extension in vitro.

One oligonucleotide analog is already on the way to perhaps becoming the first ap­proved telomerase inhibitor for treatment of cancer. Called GRN163L, it is currently in human clinical trials sponsored by Geron, Menlo Park, Calif. GRN163L is a lipid-con-jugated thiophosphoramidate. Its nucleo­tide sequence is complementary to that of telomerase's R N A template, enabling it to bind the telomerase active site and thus in­hibit the enzyme.

Geron Director and Senior Research Fellow Sergei M. Gryaznov and cowork­ers discovered GRN163L by synthesizing phosphoramidates and thiophosphorami-dates and identifying some that inhibited telomerase fairly effectively. They optimized the compounds' sequence and length, and they enhanced the analogs' ability to be absorbed by cells by conjugating them with lipophilic groups.

Gryaznov and coworkers identified GRN163L as one of their best inhibitory

END OF LINE Telomeres occur at chromosome ends. They are mostly double-stranded but also have a terminal single-stranded region at which telomerase-catalyzed extension occurs. A, T, G, and C are deoxynucleotides.

compounds. When they treated cancer cells with GRN163L, the agent caused telomere shortening and cell death without affecting the growth of normal cells. It also showed potent antitumor activity in animal models. Geron therefore selected it as a development candidate, and it is currently in Phase I and I/II clinical trials for patients with solid tu­mors and chronic lymphocytic leukemia, respectively.

Telomerase researchers are also studying immunodierapeutic agents, which stimulate an immune response against cancer cells that express telomerase. "Cancer cells pres­ent telomerase peptide fragments on their cell surfaces, where they act as antigens," Jarstfer explained, but healthy somatic cells, germline cells, and stem cells do not do this. Telomerase-based immunotherapeutics can thus immunize people against cancer cells by inducing their bodies to produce immune cells that can kill the cancer. One such vaccine developed by Geron in collabo­ration with Duke University has completed Phase I/II trials in prostate cancer patients, and an immunotherapeutic developed by Pharmexa, in Horsholm, Denmark, is go­ing into Phase II clinical trials.

WHEN TRYING to identify agents that inhibit telomerase activity selectively, it's important to consider the structural and functional aspects of the telomere, reported associate professor of medicinal chemistry Sean M. Kerwin of the University of Texas, Aus­tin. Telomere ends are known to be able to adopt four-stranded conformations called G-quadruplexes in cells, and some anti­cancer agents are being designed to bind to G-quadruplexes. Tying up the telomere's G-quadruplex could prevent telomerase from functioning properly and thus inhibit telomere lengthening.

But the telomere sequence is just one of 300,000 or so sequences in the human ge­nome that have been predicted to be capable of folding into G-quadruplexes. "About three years ago we started worrying about

other effects G-quadruplex-interactive agents might have as a result of interacting with nontelomeric G-quadruplexes or by interfering with other enzymes besides telomerase that interact with G-quadru­plex DNA," Kerwin said.

For instance, some telome­rase inhibitors also inhibit a helicase enzyme called SV40 T-antigen. This prevents T-antigen from unwinding G-quadruplex D N A during rep­lication. Therefore, "these

telomerase inhibitors might display non­specific effects on DNA replication in both cancer and normal cells, leading to toxicity," Kerwin said. "We were able to identify a few G-quadruplex-interactive agents that selec­tively inhibited telomerase and not T-anti­gen." He suggested that these would tend to be less toxic than nonselective quadruplex-interactive agents. His group's work thus has implications "for understanding the way in which different G-quadruplex-associated proteins recognize these fascinating D N A structures and how small molecules can be designed to interfere with this recognition in a very selective fashion," Kerwin said.

Researchers are also trying to better un­derstand the structural aspects of telomere folding. For example, assistant professor of pharmacology and toxicology Danzhou Yang of the University of Arizona, Tuc­son, and coworkers recently were one of two groups that determined, using nuclear magnetic resonance spectrometry, a solu­tion structure of the G-quadruplex formed by human telomeres in potassium solution (Nucleic Acids Res. 2006,34,2723; C&EN, July 31, page 46).

"Our results demonstrated a novel, unprec­edented intramolecular G-quadruplex folding topology," Yang said. The distinct folding to­pology of the structure suggests that it might be possible to target it with small-molecule drugs in a highly selective manner.

Wha t drug designers would really like to know is exactly how telomerase interacts with telomeric G-quadruplexes. Holding back such studies is that "we don't have a structure of telomerase," although partial structures have been obtained, Jarstfer said. "The main problem is obtaining large quantities of the purified [RNA-protein] complex."

Whe the r telomerase turns out to be a near-universal anticancer target remains to be seen. But with the enzyme being targeted and studies progressing in so many different ways, researchers are quickly closing in on a deeper understanding of how it works and how it can be controlled therapeutically. •

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