Method for the extraction of a factor that mediates contact inhibition of cell growth

Claim 3

The method of claim 1 wherein said hydrophobic affinity material comprises phenyl-sepharose.

Claim 4

The method of claim 2 which comprises monitoring the ultraviolet absorption spectra of the distilled water eluate from the column at 280 nM.

Claim 5

The method of claim 3 wherein said buffers of decreasing ionic strength comprise solutions of 10 mM Tris HCl containing 2 molar NaCl, 1 molar NaCl, 0.5 molar NaCl, 0.2 molar NaCl, 0.1 molar NaCl and 0 molar NaCl.

Claim 6

The method of claim 3 which comprises dialyzing the unbuffered distilled water eluate against distilled water.

Claim 7

The method of claim 5 which comprises lyophilizing the unbuffered distilled water eluate to a powder.

Claim 8

The method of claim 6 which comprises redissolving said powder in distilled water.

Claim 9

The method of claim 7 which comprises precipitating the redissolved lyophilized powder with ethanol and collecting the solid precipitate.

Claim 10

The method of claim 8 wherein said media comprises serum free conditioned media.

Claim 11

The method of claim 9 wherein said serum free conditioned media is obtained from 48 to 72 hour old cultures of contact inhibited cells maintained in the absence of serum.

Claim 12

The method of claim 10 wherein said cells are a culture of ATCC No. CRL-1479 cells.

Claim 13

The method of claim 10 wherein said sequential elution is conducted at a temperature of between about 22° and 27° C.

Claim 14

The method of claim 12 wherein said sequential elution is conducted at 25° C.

Claim 15

The method of claim 13 wherein said sequential elution comprises application of seven buffer solutions of decreasing ionic strength to said column.

Claim 16

The method of claim 14 which comprises lyophilizing said serum free conditioned media, dissolving said media in a buffer comprising 10 mM Tris.HCl, 4 M NaCl at pH 8.0, dialyzing said solution at 4° C. against said buffer, lyophilizing the dialyzed conditioned media again to form a powder and redissolving the powder in said buffer.

Claim 17

The method of claim 15 which comprises washing said phenyl-sepharose column with distilled water and with said 10 mM Tris.HCl, 4 M NaCl at pH 8.0 buffer prior to applying serum free conditioned media to said column.

Claim 18

The method of claim 16 wherein said phenyl-sepharose is prepared by cross-linking agarose with 2,3-dibromopropanol, desulphating the resulting gel by alkaline hydrolosis under reducing conditions to form a gel matrix, and reacting said matrix with a glycidyl ether.

Claim 19

The method of claim 16 which comprises monitoring the UV wavelength of the eluate from said column at 280 nM.

Claim 20

A composition comprising a contact inhibition factor that restores contact inhibition of growth to malignant mamalian cell types, said composition being prepared by applying a sample comprising media conditioned by growth of a contact inhibited cell culture to a fractionating column comprising a non-ionic hydrophobic affinity material, the hydrophobic bonding interaction of said material with proteins capable of being modified in the presence of buffers of varying ionic strength, sequentially eluting the column with buffers of decreasing ionic strength, applying unbuffered distilled water to said column after eluting with said buffers of decreasing ionic strength, collecting the material eluting with the distilled water, lyophilizing the distilled water to said column after eluting with said buffers of decreasing ionic strength, collecting the material eluting with the distilled water, lyophilizing the distilled water eluant to a powder, dissolving the lyophilized powder in distilled water to form a solution, adding ethanol to said solution to form a precipitate comprising said factor, and collecting said solid precipitate, said factor having a positive reaction in the Lowery assay for protein, being active to restore contact inhibition of growth in cultures of non-contact inhibited cells a UV peak absorbance at about 280 nm, being non-dialyzable, hydrophobic and water soluble and having a molecular weight in excess of 10,000 Daltons.

Claim 21

A composition comprising a contact inhibition factor that restores contact inhibition of growth to malignant mamalian cell types, said composition being prepared by applying a sample comprising media conditioned by growth of a contact inhibited cell culture to a fractionating column comprising a non-ionic hydrophobic affinity material, the hydrophobic bonding interaction of said material with proteins capable of being modified in the presence of buffers of varying ionic strength, sequentially eluting the column with buffers of decreasing ionic strength, applying unbuffered distilled water to said column after eluting with said buffers of decreasing ionic strength, collecting the material eluting with the distilled water, lyophilizing the distilled water to said column after eluting with said buffers of decreasing ionic strength, collecting the material eluting with the distilled water, lyophilizing the distilled water eluant to a powder, dissolving the lyophilized powder in distilled water to form a solution, adding ethanol to said solution to form a precipitate comprising said factor, and collecting said solid precipitate, said factor having a positive reaction in the Lowery assay for protein, being active to restore contact inhibition of growth in cultures of non-contact inhibited cells a UV peak absorbance at about 280 nm, being non-dialyzable, hydrophobic and water soluble and having a molecular weight in excess of 10,000 Daltons.

Claim 22

The method of restoring contact inhibition of growth to malignant cell types which comprises administering an effective dose for restoring contact inhibition of growth of the composition of claim 19 to said malignant cell types.