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Does maintaining normal tissue mechanics prevent cancer initiation? A focused evidence map separates the endpoints of 4 selected papers and reanalyzes an available tumor-count table. The selected contrasts occupy 4 classes, with 0 papers testing incident cancer after a mechanical intervention in humans. The table concerns already malignant cells: blocking-antibody pretreatment gives risk ratios of 0.4667 and 0.5 against its controls. These endpoints answer different questions; neither a smaller transplantation risk nor a human biomarker change establishes primary prevention. This is a bounded, exploratory source audit, not a systematic review or a new biological experiment.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: In a purposively selected four-paper evidence map, the coded contrasts occupy four distinct endpoint classes, only one paper starts its reprogramming program with normal primary cells, and none measures incident cancer after a mechanical intervention in humans, with all counts restricted to this selected set rather than the literature.
• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: Reanalysis of Weaver et al. (1997) Table II gives 7/16 tumor-bearing mice after blocking-antibody pretreatment of already malignant cells versus 15/16 untreated and 14/16 control-antibody mice, risk ratios 0.4667 and 0.5000, with two-sided Fisher p-values 0.005923 and 0.023333 (Holm-adjusted 0.011846 and 0.023333), while conservative simultaneous 95% risk-ratio intervals are 0.1612 to 1.1614 and 0.1625 to 1.3304 under independent-binomial sampling.

We provide an explicit rational parameter for every finite iteration cutoff. Its critical orbit remains uniformly below the usual escape radius throughout the cutoff, although an elementary growth argument proves that it eventually escapes. The contribution is a deterministic adversarial test family, a short uniform proof, and a certified finite benchmark. Integer enclosures and Arb ball arithmetic agree on 7 cases, with first-escape counts [23,61,212,815,3228,12879,51482]. Slow escape near the real parabolic cusp is established in the literature; we claim no discovery of that phenomenon or of its asymptotic law.

• Published, Reproduced, Reviewed.Published, Reproduced, Reviewed: The exact-rational benchmark parameters generated from cutoffs [1, 4, 16, 64, 256, 1024, 4096] have first critical-orbit escape iterations [23, 61, 212, 815, 3228, 12879, 51482], with all 7 counts certified and matched by integer dyadic enclosures and Arb ball arithmetic, and all 49 exact-rational control checks passing.
• Published, Reviewed.Published, Reviewed: For every integer T >= 1, the real parameter c_T = 1/4 + 1/[16(T+1)^2] has critical iterates z_0 = 0 and z_(n+1) = z_n^2 + c_T in [0,17/32] for 0 <= n <= T, but an unbounded critical orbit.

Published aggregate follow-up tables can support a transparent sensitivity calculation without reconstructing participant records or fitting the original trial model. We examined 6 long-term recovery rows from PRINCIPLE, keeping the primary and larger sensitivity cohorts separate. For the primary six-month row, the respondent-only treatment-minus-control recovery difference is 3.071 percentage points. Unrestricted binary completion of unavailable responses gives a range from -16.54 to 21.764 percentage points, whereas assigning both arms any common missing-response recovery rate gives a positive range from 2.329 to 2.896 percentage points. These are conditional bounds, not confidence intervals. They quantify how assumptions affect a crude contrast and do not identify a clinical treatment effect.

• Published.Published: In six published PRINCIPLE long-term recovery rows, unrestricted binary completion bounds permit either sign of the crude recovery contrast, every common missing-response recovery rate preserves a positive contrast, and at six months in the primary cohort a missing-treatment recovery rate 13.206 percentage points below the respondent-control anchor erases that contrast, conditional on the stated completion model.