Peptides that inhibit mitosis (ANTIMITOTICS). During the 1960's the term referred to crude extracts that inhibited cell proliferation; the activity was later attributed to PYROGLUTAMATE type oligopeptides.
A vegetative stage in the life cycle of sporozoan protozoa. It is characteristic of members of the phyla APICOMPLEXA and MICROSPORIDIA.
Endogenous or exogenous substances which inhibit the normal growth of human and animal cells or micro-organisms, as distinguished from those affecting plant growth (= PLANT GROWTH REGULATORS).

Chalones: from aqueous extracts to oligopeptides. (1/5)

The term "chalone" was coined about 40 years ago to describe endogenous growth-inhibiting factors with a tissue-specific and reversible effect. A large number of "chalones" were reported in the 1970's and early 80's. The term was, however, used rather indiscriminately and attempts at purification of the active component(s) were without success. As a result, most laboratories lost interest. Then, in the early 1980's, two different research teams demonstrated that the active growth-inhibiting constituents were N-substituted oligopeptides. In the following years, similar oligopeptides were characterized in extracts of liver, the large bowel, melanocytes, lymphocytes, and neuroblastoma, in addition to the two first ones from monomyelopoietic cells and epidermis, respectively. All peptides have a bell-shaped dose response pattern and optimal effect at very low concentrations. Several of them inhibit growth even in tumors derived from the respective organs. Preliminary studies have revealed that two of the oligopeptides alter the expression of growth- and differentiation-related genes. Quite recently, some papers are again using the term "chalone" and a short review therefore seems appropriate.  (+info)

The secreted Dictyostelium protein CfaD is a chalone. (2/5)

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Cell lineages and the logic of proliferative control. (3/5)

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A Dictyostelium chalone uses G proteins to regulate proliferation. (4/5)

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eIF2alpha kinases control chalone production in Dictyostelium discoideum. (5/5)

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Chalones are hypothetical substances that were once thought to regulate the growth and proliferation of cells, particularly in the context of wound healing. The concept of chalones was first introduced in the 1950s by British scientist Dr. G. Kingsley Noble, who proposed that these substances might be produced by cells themselves and released into the extracellular environment to inhibit further cell division.

The idea behind chalones was that they might provide a natural mechanism for controlling the growth of tissues and preventing unregulated cell proliferation, which could lead to cancer. However, despite extensive research, no definitive evidence has been found to support the existence of chalones as distinct molecular entities.

While the concept of chalones has largely fallen out of favor in modern scientific discourse, the idea of using naturally occurring or synthetic molecules to regulate cell growth and proliferation remains an active area of research in fields such as cancer therapy and tissue engineering.

Medical definitions for "spores" and "protozoan" are as follows:

1. Spores: These are typically single-celled reproductive units that are resistant to heat, drying, and chemicals. They are produced by certain bacteria, fungi, algae, and plants. In the context of infectious diseases, spores are particularly relevant in relation to certain types of bacteria such as Clostridium tetani (causes tetanus) and Bacillus anthracis (causes anthrax). These bacterial spores can survive for long periods in harsh environments and can cause illness if they germinate and multiply in a host.
2. Protozoan: This term refers to a diverse group of single-celled eukaryotic organisms, which are typically classified as animals rather than plants or fungi. Some protozoa can exist as free-living organisms, while others are parasites that require a host to complete their life cycle. Protozoa can cause various diseases in humans, such as malaria (caused by Plasmodium spp.), giardiasis (caused by Giardia lamblia), and amoebic dysentery (caused by Entamoeba histolytica).

Therefore, there isn't a specific medical definition for "spores, protozoan" as spores are produced by various organisms, including bacteria and fungi, while protozoa are single-celled organisms that can be free-living or parasitic. However, some protozoa do produce spores as part of their life cycle in certain species.

Growth inhibitors, in a medical context, refer to substances or agents that reduce or prevent the growth and proliferation of cells. They play an essential role in regulating normal cellular growth and can be used in medical treatments to control the excessive growth of unwanted cells, such as cancer cells.

There are two main types of growth inhibitors:

1. Endogenous growth inhibitors: These are naturally occurring molecules within the body that help regulate cell growth and division. Examples include retinoids, which are vitamin A derivatives, and interferons, which are signaling proteins released by host cells in response to viruses.

2. Exogenous growth inhibitors: These are synthetic or natural substances from outside the body that can be used to inhibit cell growth. Many chemotherapeutic agents and targeted therapies for cancer treatment fall into this category. They work by interfering with specific pathways involved in cell division, such as DNA replication or mitosis, or by inducing apoptosis (programmed cell death) in cancer cells.

It is important to note that growth inhibitors may also affect normal cells, which can lead to side effects during treatment. The challenge for medical researchers is to develop targeted therapies that specifically inhibit the growth of abnormal cells while minimizing harm to healthy cells.

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