brightness of the ultraviolet Lyman-Ȋ
emission (based on data from comets that
have been observed at both wavelengths).
Orbital calculations
1,6
suggest that this
comet was brighter than the brightest comet
discovered by the professional surveys for
at least six months. Why was it not seen at
visible wavelengths? Does this imply that
there are many other comparable comets just
waiting to be discovered? And, if so, should
we care?
We care about the efficiency of discover-
ing comets for many reasons. The most obvi-
ous scientific reason is that we cannot find
out where comets come from and how big
they are unless we can reduce the biases in
our observations. These biases are due to
selective discovery in certain parts of the sky
and to varying orbital and physical charac-
teristics of the comets. For our peace of
mind, it is important to know whether
comets represent 10% of the potential large
impacts on Earth (as is commonly thought)
or a much larger fraction. Many people argue
that comets dominate at the largest sizes and
that the observations set only a lower limit to
this fraction.
It has long been recognized that selection
effects influence the discovery of comets,
but the magnitude of these effects is not
well understood. A few years ago, Brandt
et al.
7,8
proposed a systematic search for
small (100-metre) comets using a technique
similar to SWAN. But instead of studying
emission from hydrogen they suggested
using emission from the OH radical (the
other fragment produced when cometary
water molecules are broken apart by sun-
light) as a characteristic marker of cometary
activity. Their proposal suffered from inade-
quate satellite time, and no comets were
found.
The comet found by Mäkinen et al. is a
prototypical example of something missed
by other people because of the strong selec-
tion effects in those other searches. A system-
atic search for comets in the inner Solar
System, using the known characteristics of
comets and searching the entire sky with
high frequency, would be extremely useful.
Although observations of emission by the
OH radical would have less of a problem with
background noise, a systematic search by
SWAN using longer integration times would
almost certainly turn up additional comets.
It would add tremendously to our knowl-
edge of the physical and orbital properties
of comets and would provide an insight into
the real statistical frequency of cometary
impacts on Earth. ■
Michael F. A’Hearn is in the Department of
Astronomy, University of Maryland, College Park,
Maryland 20742-2421, USA.
e-mail: ma@astro.umd.edu
1. Mäkinen, J. T. T. et al. Nature 405, 321–322 (2000).
2. Gehrels, T. (ed.) Hazards due to Comets and Asteroids (Univ.
Arizona Press, Tucson, 1994).
3. Grieve, R. A. F. & Shoemaker, E. M. in Hazards due to Comets
news and views
NATURE | VOL 405 | 18 MAY 2000 | www.nature.com 287
B
oth benign and malignant tumours
grow in an uncontrolled way. But it is
only cells of malignant tumours that
invade surrounding tissues and travel to
distant organs (metastasize). Conventional
wisdom used to hold that invasion and
metastasis are late events — often ‘too late’
— in the clinical course of a patient’s cancer.
However, we now know that invasion can be
both early and clinically ‘silent’. An under-
standing of the molecular basis for this
aggressiveness could lead to therapies that
block the transition of a tumour from benign
to malignant, and keep local disease in check.
Taguchi and colleagues
1
, writing on page 354
of this issue, have now identified proteins
called RAGE and amphoterin as a
receptor–ligand pair in a molecular check-
point that regulates not only the invasiveness
but also the growth and movement of
tumour cells — the trio of characteristics
required for malignancy.
The threat of tumour invasiveness is
exemplified by the fact that brain cancer
does not need to metastasize to kill a patient.
The growth of a brain tumour mass in the
Cancer
Checkpoint for invasion
Lance A. Liotta and Timothy Clair
and Asteroids (ed. Gehrels, T.) 417–462 (Univ. Arizona Press,
Tucson, 1994).
4. Bailey, M. E. et al. in Hazards due to Comets and Asteroids (ed.
Gehrels, T.) 479–533 (Univ. Arizona Press, Tucson, 1994).
5. Marsden, B. G. & Williams, G. V. Catalogue of Cometary Orbits
1999 13th edn (Minor Planet Center, Cambridge, MA, 1999).
6. Marsden, B. G. Minor Planet Electronic Circular 1999-X07
Pseudopod
Tumour
cell
Extracellular matrix
Detach Attach Pseudopod
protrusion
Motility
Invasion
Proteolysis
Growth
RAGE Amphoterin
Actin
mobilization
p42/p44
JNK
p38
Intercellular adhesion
molecules
Cell–matrix adhesion
molecules
Actin filaments
Figure 1 Spatial and temporal regulation of cellular invasion of the extracellular matrix. Invasion
can be normal (for example, in the case of the outgrowth of neuronal protrusions during brain
development) or malignant (for example, in the case of tumours). Top, invasion can be viewed as
cellular motility coupled to regulated adhesion and detachment (from the extracellular matrix) and
proteolysis (of extracellular matrix molecules). The advance of pseudopods (extensions) of the cell —
driven by the formation of actin polymers, a component of the cytoskeleton — may require the
action of cell-surface protein-degrading enzymes, as well as other enzymes, receptors and activators.
Extracellular matrix degradation must be balanced by antiproteolysis (that is, processes that inhibit
proteolysing enzymes) to allow for adhesive traction. Bottom, signal-transduction pathways allow
the individual cell to move between phases of pseudopod protrusion, extracellular matrix
degradation, antiproteolysis, adhesion and detachment. These pathways split at the level of the
mitogen-activating protein kinases JNK, p38 and p42/p44. Blocking the interaction between
amphoterin and RAGE suppresses these pathways, as shown by Taguchi et al.
1
.
(Minor Planet Center, Cambridge, MA, 1999).
7. Brandt, J. C. et al. Earth, Moon and Planets 72, 243–249
(1996).
8. Brandt, J. C. et al. in Completing the Inventory of the Solar
System (eds Rettig, T. W. & Hahn, J. M.) 289–297 (Astron. Soc.
Pacific, San Francisco, 1996).
9. http://www.geo.fmi.fi/PLASMA/SWAN
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