Cell Language Theory, The: Connecting Mind And Matter

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314 The Cell Language Theory: Connecting Mind and Matter

b2861 The Cell Language Theory: Connecting Mind and Matter “6x9”

There appear to exist common mRNA phenotypes (i.e., mRNA dissi-
patons) that are closely associated with breast cancer. (7.21)

One experimental support for Statement (7.21) is provided by the fact
that any one of the four mechanism phenotypes, i.e., 2, 4, 6, and 8, can be
associated with or “realized by” two or more genes either within a given
patient (see columns in Figure 7.12) or in different patients (see rows in
Figure 7.12). The difference between genes and RNA phenotypes (e.g.,
mechanism phenotypes defined in Figure 7.11) may be compared with the
difference between words and their meanings. The same meaning can be
conveyed by two or more different words. This is equivalent to saying that
two signs can have the same meaning (or interpretant to use the Peircean
idiom; see Section 6.3 and Figure 9.1). The RNA phenotypes (also called
RNA trajectories, RNA expression profiles, RNA dissipative structures, or
RNA dissipatons, mechanism phenotypes) found in individual breast cancer
patients may be referred to as the patient-specific breast cancer-associated
RNA profiles or patient-specific breast cancer-associated RNA dissipatons.

(3) There are no continuous, unbroken vertical strips of either color, red
or green, in Figure 7.12. This observation, when combined with the
ICFI hypothesis described in Section 3.2.1, can lead to the following
conclusion:

There are no breast cancer patients for whom doxorubicin is 100%
beneficial or 100% harmful. (7.22)

In other words,

The therapeutic efficacy of doxorubicin depends on breast cancer patients.
(7.23)

If Statement (7.23) can be generalized, Statement (7.24) would result:

The therapeutic efficacy of anticancer drugs depend on individual
cancer patients. (7.24)

If Statement (7.24) can be substantiated by further studies, it would
provide the empirical basis for advocating the necessity for personalized
medicine (see Figure 7.2c), in contrast to “group” or “average” medicine.

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