Headlines at Hopkins: news releases from across the 
university Headlines
News by Topic: news releases organized by subject News by Topic
News by School: news releases organized by the 
university's 9 schools & divisions News by School
Events Open to the Public (campus-wide) Events Open
to the Public
Blue Jay Sports: Hopkins Athletic Center Blue Jay Sports
Search News Site Search the Site

Contacting the News Staff: directory of university 
press officers Contacting
News Staff
Receive News Via Email (listservs) Receive News
Via Email
Resources for Journalists Resources for Journalists

Virtually Live@Hopkins: audio and video news Virtually
Hopkins in the News: news clips about Hopkins Hopkins in
the News

Faculty Experts: searchable resource organized by 
topic Faculty Experts
Faculty and Administrator Photos Faculty and
Faculty with Homepages Faculty with Homepages

JHUNIVERSE Homepage JHUniverse Homepage
Headlines at Hopkins
News Release

Office of News and Information
Johns Hopkins University
3003 N. Charles Street, Suite 100
Baltimore, Maryland 21218-3843
Phone: (410) 516-7160 | Fax (410) 516-5251

Embargoed until 12:45 p.m. EDT
Tuesday, August 22, 2000
CONTACT: Michael Purdy

Molecular Architects Create New Cancer Preventives

Researchers at The Johns Hopkins University have developed a modified form of vitamin D and determined that it helps delay the onset and reduce the number of skin cancers in lab mice. Unlike vitamin D, though, the new compound does not cause calcium to seep from the bones.

If not for the calcium loss problem, large doses of vitamin D could be used to reduce the odds of developing cancer in patients whose medical history, genetic heritage, or environmental exposures put them at increased risk. Depending on the results of further tests in animals and potential tests in humans, the new compound and others to follow it may provide an important alternative approach to reducing cancer risk for such patients.

Gary Posner, Scowe Professor of Chemistry in Hopkins' Krieger School of Arts and Sciences and one of the new compound's creators, will describe work to design and test the compounds at a meeting of the American Chemical Society in Washington, D.C. this week.

Chemistry Professor Gary Posner and graduate student Ken Crawford, at work in the lab, have designed compounds similar to vitamin D that retain the beneficial effects of the vitamin but lack its hazards.

In the July/August issue of Carcinogenesis, Posner and Thomas Kensler, professor at the Johns Hopkins School of Public Health, published results of tests in mice of four modified forms of vitamin D, called deltanoids or vitamin D analogs. The deltanoids were applied to the skin of mice also treated with a carcinogen.

All four deltanoids diminished the number of skin tumors without any significant effects on calcium loss or weight gain, which is usually adversely affected by vitamin D. The most effective preventive compound was a doubly modified 'hybrid' compound that contained fluorine.

The new deltanoids are, for the most part, identical to vitamin D, which is normally generated in the skin during exposure to sunlight. In several areas, though, Posner and his students have given the compounds' molecular structures several small 'tweaks.'

'We call our work molecular architecture, because at the submicroscopic level we are altering the structures of known compounds or designing new compounds from scratch,' explains Posner.

Crawford holds a sample of the vitamin D analog that tested best in mice for ability to reduce the chances of getting cancer without promoting calcium loss in bones.

Those alterations can include adding components to, taking things away from, and re-orienting parts of the molecule.

'It's still a science and an art combined,' Posner explains. 'It's not yet possible for anyone to go from a new chemical structure and to predict in advance the biological properties of that new structure.'

This inability of molecular architects to predict exactly the results of their design changes can sometimes force them to rely on their intuitive sense of which change will produce the desired result. But the design process is also rational, Posner emphasizes, because it is based to the greatest extent possible on principles established through prior experimentation. Earlier research in the deltanoids included many efforts by pharmaceutical companies to improve vitamin D.

'What we did was to take some of the best structural changes that large pharmaceutical companies have made public,' Posner says, 'and incorporated those changes with a structural change that we discovered here 10 years ago in a different portion of the molecule.'

Posner's group found that if they added a methylene group, composed of one extra carbon atom and two hydrogen atoms, to an area of the vitamin D molecule known as the A ring, the molecule caused much less calcium loss.

Based on the research of another lab, Posner's group also added two fluorine atoms to the molecule at an ideal point to reduce the body's ability to break down and metabolize the vitamin D analogs. This not only reduces the levels of potentially harmful metabolites produced by the analogs, it also keeps the analogs active in the body longer.

The changes are all small compared to the size of the vitamin D molecule, which has a total of 27 carbon atoms. But they make a significant difference in its effects. 'You might think you'd have to change large portions of the molecule to change its biological effects, but it's well-known that you can do that by changing small portions of the molecule,' Posner says.

Further animal tests of the analog on different types of tumors are planned in Kensler's lab. If the new tests and tests in humans prove successful, doctors might one day be able to consider treating patients at high risk for cancer with the compound, probably applying it as a topical gel.

Meanwhile, Posner's lab is already at work on yet another generation of improved deltanoids.

'There's a lot of trial and error,' he says. 'My research group has, over the years, made about 100 different vitamin D analogs. And the winners are probably limited to 10. If you consider the more general issue in the pharmaceutical industry, though, going from the bench to a drug-typically it's one in many thousands of compounds. And that gives you a feeling for just how far rational design can or can't come.'

This research was funded in part by grants from The National Cancer Institute of the National Institutes of Health.

Related Audio Files
Listen to Gary Posner

"As organic chemists, we call ourselves really molecular architects...at the sub-microscopic level, we are altering the structures of compounds, either altering known compounds or designing new compounds from scratch, and preparing them in the chemical laboratory for biological evaluation." (15.42 seconds)
Listen [wav file]
Listen [RealAudio file]

"These analogs and especially the hybrid analog are not only efficacious in preventing tumor formation, delaying tumor formation, diminishing the number of tumors, but they also don't harm the animals, even when administered at levels at which the natural hormone is well-known to be toxic." (19.076 seconds)
Listen [wave file]
Listen [RealAudio file]

"You might think you'd have to change large portions of the molecule to change the biological profile, but it's well-known that generally you can change minute portions and get quite different biological responses." (14.403 seconds)
Listen [wav file]
Listen [RealAudio file]

You'll need a RealPlayer to watch or listen to these audio
and video presentations. Download one for free here.

For questions or comments on these Real Presentations,
e-mail glenn@jhu.edu.


Johns Hopkins University news releases can be found on the World Wide Web at http://www.jhu.edu/news_info/news/
   Information on automatic e-mail delivery of science and medical news releases is available at the same address.

Go to Headlines@HopkinsHome Page