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babunello [35]
1 year ago
6

senescence-like phenotype distinguishes tumor cells that undergo terminal proliferation arrest after exposure to anticancer agen

ts.
Biology
1 answer:
Artist 52 [7]1 year ago
8 0

Senescence-like phenotype is normally regarded as a suppressive manner, both by preventing cancer cellular proliferation and suppressing malignant development from pre-malignant to malignant disorder.

Senescence is generally regarded as a tumour suppressive method, both with the aid of preventing cancer cell proliferation and suppressing malignant progression from pre-malignant to malignant disease. Cell senescence limits the replicative potential of cells, as a consequence stopping the proliferation of cells which are at distinct stages of malignancy.

A recent frame of evidence shows that induction of senescence can be exploited as a foundation for most cancers therapy. Senescence is a double-edged sword which could function in contrary directions. It far a capacity mechanism for a cell to avoid malignant transformation. however, senescence can also sell most cancers improvement with the aid of changing the cellular microenvironment thru a senescence-related secretory phenotype.

Learn more about phenotype here:-brainly.com/question/902712

#SPJ4

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I need help with this biology question pls and thankyou pls help
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The answer to this question is #2 it has guanine and ribose!
4 0
2 years ago
Based on the definitions of pharmacophore and privileged structure, outline essential structural features a 1,4-dihyrdopyridine
stiv31 [10]

Answer:

Explanation:

Pharmacophore (pharmacology) - The molecular framework responsible for a drug's biological activity. According to IUPAC — A pharmacophore is the ensemble of steric and electronic features that is necessary to ensure the optimal supramolecular interactions with a specific biological target structure and to trigger (or to block) its biological response.

Privileged structures are defined as molecular frameworks which are able of providing useful ligands for more than one type of receptor or enzyme target by judicious structural modifications.

1) The 1,4-dihydropyridine ring is present in many biologically important molecules that acts as an important scaffold for cardiovascular drug - a calcium antagonists and although it is technically not considered as a pharmacophore, it is considered as a privileged structure.

1,4-Dihydropyridine (DHP), belongs to the class of calcium antagonist that inhibits the influx of extracellular Ca+2 through the L-type voltage-dependent calcium channels.

A positional substitution in the 4-position is feasible in the heterocyclic ring which in turn culminates in various calcium channel antagonist activities and this heterocyclic ring is the common feature for various pharmacological activities such as anti-inflammatory activity, analgesic activity,

antihypertensive, antianginal, antitumor, antitubercular activity and antithrombotic .

Position on the heterocyclic ring binds to the L-type channel and also to N-type channel on membranes.

2.) The bioisosteres are not a suitable bioisostere for the traditional C-4 aryl or heteroaryl substitution which is necessary for calcium ion blockage thereby inhibiting it to function with the mechanism shared above.

6 0
3 years ago
A student lives in a home some few miles from a nearby coal crushing site. The vegetation and structures within the
Gnesinka [82]
The correct answer is C
7 0
2 years ago
What 2 processes must occur in order for new cells to reproduce?
Aleks [24]

Answer:

mitosis and meosis

4 0
2 years ago
Why does the sodium potassium pump require ATP?
SpyIntel [72]

Answer:

The sodium–potassium pump is found in many cell (plasma) membranes. Powered by ATP, the pump moves sodium and potassium ions in opposite directions, each against its concentration gradient. In a single cycle of the pump, three sodium ions are extruded from and two potassium ions are imported into the cell.

Explanation:

Hope I helped!

5 0
2 years ago
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